АкушерствоАнатомияАнестезиологияВакцинопрофилактикаВалеологияВетеринарияГигиенаЗаболеванияИммунологияКардиологияНеврологияНефрологияОнкологияОториноларингологияОфтальмологияПаразитологияПедиатрияПервая помощьПсихиатрияПульмонологияРеанимацияРевматологияСтоматологияТерапияТоксикологияТравматологияУрологияФармакологияФармацевтикаФизиотерапияФтизиатрияХирургияЭндокринологияЭпидемиология

Приложение 8. 239 14 страница

Прочитайте:
  1. B)новокаинмен жансыздандыру 1 страница
  2. B)новокаинмен жансыздандыру 2 страница
  3. B)новокаинмен жансыздандыру 3 страница
  4. B)новокаинмен жансыздандыру 4 страница
  5. B)новокаинмен жансыздандыру 5 страница
  6. B)новокаинмен жансыздандыру 6 страница
  7. B)новокаинмен жансыздандыру 7 страница
  8. D. Латеральна огинаюча стегно і стегнова 1 страница
  9. D. Латеральна огинаюча стегно і стегнова 10 страница
  10. D. Латеральна огинаюча стегно і стегнова 2 страница

2093. Juda A. (1953). Höchstbegabung, ihre Erbverhältnisse sowie ihre Beziehungen zu psychischen Anomalien, Urban and Schwarzenberg, München, Berlin.

2094. Juel-Nielsen N., Harvard B. (1958). The electroencephalogram in monovular twins brought up apart, Acta Genet. (Basel), 9, 57-64.

2095. Juel-Nielsen N. (1965). Individual and environment, A psychiatric-psychological investigation of monozygotic twins reared apart, Acta Psychiatr. Scand. [Supp.], 183.

2096. Just G. (1970). Erbpsychologie der Schulbegabung. In: Handbuch der Erbbiologie des Menschen, Just G. (ed.), Vol. V/l, Springer, Berlin, pp. 538-591.

2097. Kaij L. (1960). Alcoholism in twins, Almquist and Wiksell, Stockholm.

2098. Kallman F. J. (1953). Heredity in health and mental disorder, Norton, New York.

2099. Kalmus H., Fry D.B. (1980). On tune deafness (dysmelodia): frequency, development, genetics and musical background, Ann. Hum. Genet, 43, 369-382.

2100. KaropkaR.J., Benzer S. (1971). Clock mutants of Drosophila melanogaster, Proc. Natl. Acad. Sei. USA, 68, 2112-2116.

2101. Kay D. W.K. (1963). Late paraphrenia and its bearing on the aetology of schizophrenia, Acta Psychiat Scand., 39, 159-169.

2102. KendlerK.S. (1983). Overview: A current perspective on twin studies of schizophrenia, Am. J. Psychiat, 140, 1413-1425.

2103. Kety S.S. (1959). Biochemical theories of schizophrenia, Science, 129, 1528-1532.

2104. Kety S.S., Rosenthal D., Wender P.H., Schulsinger F., Jacobsen B. (1975). Mental illness in the biological and adoptive families of adopted individuals who have become schizophrenic. In: Genetic research in psychiatry, Fiere R. R., Rosenthal D., Brill N. (eds.), Johns Hopkins Press, Baltimore, p. 147.

2105. Knorring A.L. v., Cloninger R., Behman M.,


Литература


Siqvardsson S. (1983). An adoption study of depressive disorders and substance abuse, Arch. Gen. Psychiatr., 40, 943-950.

2106. König K. (1959). Der Mongolisme, Hippokrates, Stuttgart.

2107. Krech D., Rosenzweig M. R., Bennet E. L., Kraeckel B.A. (1954). Enzyme concentrations in the brain and adjustive dehavioral patterns, Science, 120, 994-996.

2108. Kringlen E. (1967). Heredity and environment in the functional psychoses, Heinemann, London.

2109. Krüger J., Propping P. (1976). Rückgang der Zwillingsgeburten in Deutschland, Dtsch. Med. Wochenschr., 101, 475-480.

2110. Kuhlo W., HeintelH., Vogel F. (1969). The 4-5/sec. rhythm, EEG Clin. Neurophysiol., 26, 613-619.

2111. Lauer J., Lindauer M. (1971). Genetisch fixierte Lerndispositionen bei der Honigbiene, Inf. Org. l, Akademie der Wissenschaft und Literatur, Mainz.

2112. Lauer J., Lindauer M. (1973). Die Beteiligung von Lernprozessen bei der Orientierung, Fortschr. Zool., 21, 349-370.

2113. Lenz F. (1932). Menschliche Auslese und Rassenhygiene. In: Bauer E., Fischer E., Lenz F. Menschliche Erblichkeitslehre und Rassenhygiene, Lehmann, München.

2114. Leonhard K. (1957). Aufteilung der endogenen Psychosen, 1st ed., Académie-Verlag, Berlin.

2115. Lester D., Freed E. X. (1972). A rat model of alcoholism. In: Nature and nurture in alcoholism, Ann. N.Y. Acad. Sei., 197, 54-59.

2116. Lewis E.O. (1933). Types of mental deficiency and their social significance, J. Ment. Sei., 79, 298.

2117. Lewontin R. С. (1975). Genetic aspects of intelligence, Ann. Rev. Genet, 9, 387-405.

2m&.LippH.P., SchweglerH., Driscoll P. (1984). Postnatal modification of hippocampal circuity alters avoidance learning in adult rats, Science, 225, 80-82.

2118. Little A. J. (1974). Psychological characteristics and patterns of crime among males with an XYY sex chromosome complement in a maximum security hospital, B.A. Sp. Hon. Thesis (Quoted from Borgaonkar and Shan), Sceffield University.

2119. LoehlinJ.C. (1980). Recent adoption studies of I. Q., Hum. Genet., 55, 297-302.

2120. Loehlin J.C., Lindzey G., Spuhler J.N. (1975). Race differences in intelligence, Freeman, San Francisco.

2121. Lubs H. A. (1983). X-linked mantal retardation and the marker X. In: Emery A. E. H., Rimoin D. L. (eds.), Principles and Practice of Medical Genetics, Churchill Livingstone, Edinburgh etc., pp. 216-223.

2122. Manosevitz M., Lindzey G. (1969). Thiessen D. D., Behavioral genetics: methods and research, Appleton-Century-Crofts, New York.

2123. MarsdenC.D. (1982). Neurotransmitters and DNS disease: Basal ganglion disease, Lancet, П, 1141-1146.


 

2124. Matthyse S., Spring B.J., Sugorman J. (eds.) (1978). Attention and information processing in schizophrenia, J. Psychiat. Res., 14, 1-331.

2125. Maubach M., Diebold K., Friedl W., Propping P. (1982). M АО-Aktivität in Thrombocyten von affektpsychotischen Patienten und ihren Verwandten ersten Grades. In: Beckmann H. (ed.), Biologische Psychiatrie, Thieme Verlag, Stuttgart-New York, pp. 182188.

2126. McClearn G.E. (1972). Genetics as a tool in alcohol research. In: Nature and nurture in alcoholism, Ann. N.Y. Acad. Sei., 197, 26-31.

2127. McClearn G. E., Rodgers D. A. (1972). Differences in alcohol preference among inbred strains of mice, Q. J. Stud. Alcohol., 20, 691-695.

2128. McGwire L.S., Ryan K.O., Omenn G.S., (1975). Congenital adrenal hyperplasia. II. Cognitive and behavioral studies, Behav. Genet, 5, 175-188.

2129. Mendels J., Stern S., Frazer A. (1976). Biochemistry of depression, Dis. Nerv. Syst, 37, 4-36.

2130. Mednik S.A., Mura E., Sculsinger F., Mednik B. (1973). Perinatal conditions and infant development in children with schizophrenic parents, Soc. Biol., 20, 111-112.

2131. Mendlewicz J., Rainer J. D. (1977). Adoption study supporting genetic transmissions in manic-depressive illness, Nature, 268, 327-329.

2132. Migeon В., DerKaloustian V.M., Nyhan W.L., Young W.J., ChildsB. (1968). X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: Hétérozygote has two clonal populations, Science, 160, 425-427.

2133. Money J. (1968). Cognitive deficits in Turner's syndrome. In: Progress in human behavior genetics, Vandenberg S. (ed.), Johns Hopkins Press, Baltimore, pp. 27-30.

2134. Money J., Alexander D. (1966). Turner's syndrome: Further demonstration of the presence of specific congnitional deficiencies, J. Med. Genet, 3, 47.

2135. Motulsky A. G. (1979). Possible selective effects of urbanization on Ashkenazi Jewish populations. In: Genetic Diseases among Ashkenazi Jews, Goodman R. M., Motulsky A. G. (eds.), Raven, New York, pp. 201-212.

2136. Motulsky A.G. Ashkenazi Jewish gene pools: admixture, drift and selection. In: Population genetic studies on isolates, Sigrid Juselius Symposium VII, Academic Press, London, pp. 353-365.

2137. Motulsky A.G. (1981). Some research approaches in psychiatric genetics. In: Genetic Strategies in Psychobiology and Psychiatry, Gershon E. L., Matthysse S., Breakefield X. O., Ciranello R.D. (eds.), The Boxwood Press, Pacific Grove, C.A., pp. 423-428.

2138. Müller-Kuppers M., Vogel F. (1965). Über die Persönlichkeitsstruktur von Trägern einer seltenen erblichen EEG-Variante, Jahrb. Psycholog. Psychother. Med. Anthropol., 12, 75-101.


Литература 311


2139. Muller H. J. (1925). Mental traits and heredity, J. Hered., 16, 433-448.

2140. Murken J.D. (1973). The XYY-syndrome and Klinefelter's syndrome, Topics Human Genetics, Thieme, Stuttgart.

2141. Myrianthopoulos N. C., Nichols P. L., Broman S.H. (1976). Intellectual development of twins-comparison with singletons, Acta Genet. Med. Gemellol (Roma), 25, 376-380.

2142. Nachtsheim H. (1959). Probleme vergleichender Genetik bei Saugern, Naturwissenschaften, 20, 565-573.

2143. Neisser U. (1976). Academic and artificial intelligence. In: The Nature of Intelligence, Resnick L. B. (ed.), Erlbaum, Hillsdale, pp. 135-144.

2144. Nielsen J. (1970). Criminality among patients with Klinefelter's syndrome, Br. J. Psychiatry, 117, 365-369.

2145. Nielsen J., Hreidersson A.B., Christensen K. R. (1973). D/£> translocations in patients with mental illness, Hereditas, 75, 131-135.

2146. Nielsen J., Sillesen I., Sfrensen A.M., S</>rensen K. (1979). Follow-up until age 4 to 8 of 25 unselected children with sex chromosome abnormalities, compared with sibs and controls, Birth Defects: Original Article Series, Vol. XY, pp. 1573.

2147. Nielsen J., Sfrensen A.M., Sjrensen K. (1981). Mental development of unselected children with sex chromosome abnormalities, Hum. Genet., 59, 324-332.

2148. Noel В., Duport J. P., Revil D., Dussuyer L, Quack B. (1974). The XYY symdrome: Reality or myth? Clin. Genet., 5, 387-394.

2149. Отели G. S., Wade Cohen P. T., Motulsky A. G. (1977). Genetic variation in glycolytic enzymes in human brains, International Congress of Human Genetics, Experta Medica, Paris, 1977, International Congress, Series. 233: 135.

2150. Omenn O.S., Weber B.A. (1978). Dyslexia: search for phenotypic and genetic heterogeneity, Am. J. Med. Genet, 1, 333-354.

2151. OpitzJ.M., Sutherland G.R. (eds.) (1984). Conference report: International workshop on the fragile X and X-linked mantal retardation, Am. J. Med. Genet, 17, 5-385.

2152. Overton W.F. (1973). On the assumptive base of the nature-nurture controversy: Additive versus interactive conceptions, Hum. Dev., 16, 74-89.

2153. Parker N. (1964). Twins: A psychiatric study of a neurotic group, Med. J. Aust, 51, 735742.

2154. Partanen J., Bruun K., Markkanen T. (1966). Inheritance of drinking behavior. The Finnish Foundation for Alcohol Studies, Vol. 14.

2155. Paul J., Froster-lskenius U., Moje W., Schwinger E. (1984). Heterozygous female carriers of the marker-X-chromosome: I. Q. estimation and replication status of fra(X)(q), Hum. Genet, 66, 344-346.

2156. Penrose L.S. (1938). (Colchester survey) A clinical and genetic study of 1280 cases of mental


defect, Spec. Rep. Ser. Med. Res. Counc. (London), 229, His Maj Stat Off., London.

2157. Penrose L.S. (1962). The biology of mental defect, 3rd ed., Grüne and Stratton, New York.

2158. Pollock V.E., Volavka J., Goodwin D. W., MednikS.A., GabrielliW.F., Knop J., Schulsinger F. (1983). The BEG after alcohol administration in men at risk for alcoholism, Arch, of Gen. Psychiat, 40, 857, 861.

2159. Popenoe P. (1922). Twins reared apart, J. Hered., 5, 142-144.

2160. Praag van H.M. (1982). Neurotransmitters and CNS disease: Depression, The Lancet, II, pp. 1259-1264.

2161. Propping P. (1977). Genetic control of ethanol action on the central nervous system, Hum. Genet., 35, 309-334.

2162. Propping P. (1978). Alcohol and alcoholism. In: Human genetic variation in response to medical and environmental agents: Pharmacogenetics and ecogenetics, Motulsky A. G. et al. (eds.), Hum. Genet, Suppl. 1, 91-99.

2163. Propping P. (1980). Genetic aspects of alcohol action on the electroencephalogram (EEG). In: Biological research in alcoholism, Begleiter H., Kissin (eds.), Plenum, New York, pp. 589-602.

2164. Propping P. (1983). Genetic disorders presenting as "schizophrenia", Karl Bonhoeffer's early view of the psychoses in the light of medical genetics, Hum. Genet, 65, 1-10.

2165. Propping P., Friedl W. (1983). Genetic control of adrenergic receptors on human platelets. A twin study, Hum. Genet, 64, 105-109.

2166. Propping P., Friedl W. (1983). Platelet MAO activity and high risk for psychopathology in a German population, Mod. Probl. Pharmacopsychiat, 19, 304-314.

2167. Propping P., Krüger J., Mark N. (1981). Genetic disposition to alcoholism. An EEG study alcoholics and their relatives, Hum. Genet, 59, 51-59.

2168. Propping P., Friedl W., Nebel В., Feige A. (1979). Plasma DBH platelet MAO and proteins of red blood cell membranes in individual with variants of the normal EEG, Neuropsychology, 169, 5, 309-316.

2169. Propping P., Корин M. (1973). Pharmacogenetic aspects of psychoreactive drugs: facts and fancy, Hum. Genet, 20, 291-320.

2170. Puck M.H. (1981). Some considerations bearing on the doctrine of self-fulfilling prophecy in sex chromosome aneuploidy, Am. J. Med. Genet, 9, 129-137.

2171. Puck M.H., Bender B.G., BorelliJ.B., SalbenblattJ.A., Robinson A. (1983). Parent's adaptation to early diagnosis of sex chromosome anomalies, Am. J. of Med. Genet, 16, 71-79.

2172. QuaziR.H., Reed Т.Е. (1975). A possible major contribution to mental retardation in the general population by the gene for microcephaly, Clin. Genet, 7, 85-90.

2173. Rao D.C., Morton N. E., Eiston R.C., Гее S.


312 Литература


(1977). Causal analysis of academic perfor- 2190. mance, Behav. Genet, 7, 147-159.

2174. Ratcliffe S.G. (1982). Speed and learning disorders in children with sex-chromosome 2191. abnormalities, Developm. Med. and Child Neurolog., 24, 80-84.

2175. Ratcliffe S. G., Field M. A. S. (1982). Emotional 2192. disorders in XYY children: Four case reports,

J. Child Psychol. Psychiatr., 23, 401-406.

2176. Ratcliffe S.G., Tierney I., Nshaho J., Smith L., Springbett Α., Gallon S. (1982). The Edinburgh 2193. study of growth and development of children

with sex-chromosome abnormalities, Birth Defects, Original Article Series, 18(4), 41- 2194. 60.

2177. Reed Т.Е., Kalant H., Gibbins R.J., KapurB.M., Rankin J. G. (1976). Alcohol and aldehyde metabolism in Caucasians, Chinese 2195. and Amerinds, Can. Med. Assoc. J., 115, 851-855.

2178. Renpenning H., GerrardJ.W., Zaleski W.A., 2196. Tabata T. (1962). Familial sex-linked mental retardation, Canad. Med. Ass. J., 87, 954-956.

2179. Risch N.. Baron M. (1982). X-linked and ge- 2197. netic heterogeneity in bipolar-related major affective illness: Reanalysis of linkage data,

Ann. Hum. Genet., 46, 153-166.

2181. RodgersD.A. (1970). Mechanism-specific behavior: An experimental alternative. In: 2198. Contributions to behavior-genetic analysis.

The mouse as a prototype, Appleton-Century-Croft, New York, pp. 207-218.

2182. RodgersD.A., McClearn.G.E., Bennett E.L., 2199. Herbst M. (1963). Alcohol preference as a function of its caloric utility in mice, J. Сотр. 2200. Phys. Psychol., 56, 666-672.

2183. Rosenthal D. (ed.) (1963). The Genain quadrup- 2201. lets, Basic Books, New York, London.

2184. Rosenthal D., Wender P.H., Kety S.S., Schulsinger F., Weiner J., Qstergaard L. (1968). Schizophrenics' offspring reared in adoptive homes. In: The transmission of schizophrenia, 2202. Rosenthal D., Kety S. (eds.), Pergamon, Oxford, p. 377. 2203.

2185. Rothenbuhler N. (1964). Behavior genetics of nest cleaning in honey bees. 4. Responses of f! and back-cross generations to disease-killed brood, Am. Zool., 4, 111-123. 2204.

2186. Rüdin E. (1916). Studien über Vererbung und Entstehung geistiger Störungen, Springer, Berlin. 2205.

2187. Rüdin E. (1953). Ein Beitrag zur Frage der Zwangskrankheit, insbesondere ihrer hereditären Beziehungen, Arch. Psychiatr. Z. Neu- 2206. rol., 191, 14-54.

2188. Sounders J.B. (1982). Alcoholism: new evidence for a genetic contribution, Br. Med., J., 284, 2207. 1137-1138.

2188a.Scarr S. (1981). Race, social class, and individual differences in I.Q., Erlbaum, Hillsdale.

2189. Scarr S., Pakstis A. J., Katz S. H., Barker U. B. (1977). Absence of a relationship between degree of white ancestry and intellectual skills 2208. within a black population, Hum. Genet, 39, 69-86.


Scarr S., Weinberg R. A. (1976). I.Q. test performance of black children adopted by white families, Am. Psychol., 31, 726-739. Seixas F. A., Omenn G. S., Burk E. D., Eggleston S. (eds.) (1972). Nature and nurture in alcoholism, Ann. N.Y. Acad. Sei., 197. Severson J. A., Randall P. K., Finch C. E. (1981). Genotypic influences on striatal dopaminergic regulation in mice, Brain Res., 210, 201-215.

Shaffer J. W. (1962). A specific cognitive deficit observed in gonadal aplasia (Turner's syndrome), J. Clin. Psychol., 18, 403-406. SheppardJ.R., Albersheim В., McClearn G.E. (1970). Aldehyde dehydrogenase and ethanol preference in mice, J. Biol. Chem., 245, 2876-2882.

Shields J. (1962). Monozygotic twins brought up apart and brought up together, Oxford University Press, London. Shuey A.M. (1966). The testing of negro intelligence, 2nd ed., Social Science Press, New York.

Siervogel R.M., Weinshilboum R., Wilson A. F., E Is ton R. C. (1984). Major gene model for the inheritance of catechol-O-methyltransferase activity in five large families, Am. J. Med. Genet, 19, 315 323.

Sidman R.L., Greene M. С. (1970). Nervous new mutant mouse with cerebellar disease. In: Les mutants pathologiques chez l'animal, С. N. R. S. Paris, p. 69-79. Slater £.(1964). Genetic factors in neurosis, Brit. J. Psychol., 55, 265-269. Smythies J. R. (1976). Recent progress in schizophrenia research, Lancet, П, 136-139. Soudek D., Partington M. W., Lawson J. S. (1984). The fragile X syndrome I: Familial variation in the proportion of lymphocytes with the fragile site in mammales, Am. J. Med. Genet, 17, 241-252.

Sutherland G.R. (1983). The fragile X chromosome, Intern. Rev. Cytol., 81, 107-143. Sutherland G. R, Murch A. R., Gardiner A. J., Carter R. F., Wiseman С. (1976). Cytogenetic survey of a hospital for the mentally retarded, Hum. Genet, 34, 231-245. Schepank H. (1974). Erb- und Umweltsfaktoren bei Neurosen, Springer, Berlin Heidelberg, New York.

Schmid W, Nielsen J. (eds.) (1981). Human Behavior and Genetics, Amsterdam, Eisevier North Holland, New York, Oxford. Schulsinger F. (1972). Psychopathy, heredity, and environment, Int. J. Ment, Health, 1, 190-206.

Schweigler H., Lipp H.-P. (1983). Hereditary covariations of neuronal circuity and behavior: Correlations between the proportions of hippocampal synaptic fields in the regio inferior and two-way avoidance in mice and rats, Behavioral Brain Res., 7, 1-38. Schwegler H., Lipp H.-P., Van der Loos H., Busebnaier W. (1981). Individual hippocampal mossy fiber distribution in mice correlates


Литература 313


with two-way avoidance performance, Science, 214, 817-819.

2209. Stocks P. (1930). A biométrie investigation of twins and their brothers and sisters, Ann. Eugen, 4, 49-108.

2210. Street D. R. K., Watson R. A. (1969). Patients with chromosome adnormalities in Rampton Hospital. In: Criminological implications of chromosome abnormalities, West D. J. (ed.), Cropwood Round Table Conference, Institute of Criminology, University of Cambridge, pp. 61-67.

2211. Strömgren E. (1967). Neurosen und Psychopathien. In: Humangenetik, ein kurzes Handbuch, Becker P. E. (ed.), Vol. V/2, Thieme, Stuttgart, pp. 578-598.

2212. Sturtevant A. H. (1915). Experiments of sex recognition and the problem of sexual selection in Drosophila. J. Anim. Bahav., 5, 351-366.

2213. Tariverdian G., Weck B. (1982). Nonspecific X-linked mental retardation. A review, Hum. Genet., 62, 95-109.

2214. Taylor H.F. (1980). The I.Q. game. A methodological inquiry into the heredity-environmet controversy, The Harvester Press, Brighton.

2215. Terman L.M., Merrill M.A. (1937). Measuring of intelligence, Houghton, Mifflin, Boston.

2216. Terman L.M., Oden M. H. (1959). Genetic studies of genius, Vol. V, The gifted group at midlife, Stanford University Press, Stanford (Cal).

2217. Tienari P. (1963). Psychiatric illnesses in identical twins, Acta Psychiatr. Scand. [Suppl.], 171.

2218. Tienari P. (1971). Schizophrenia and monozygotic twins, Psychiatria Fennica 1971, 97-104, Helsinki University General Hospital, Helsinki.

2219. Tsuboi T. (1970). Crimino-biologic study of patients with the XYY syndrome and Klinefelter's syndrome, Hum., Genet, 10, 68-84.

2220. Turner G., Jacobs P.A. (1984). Mental retardation and the fragile X, Adv. Hum. Genet., 13.

2221. Tyler L. E. (1976). The intelligence we test-An evolving concept. In: The nature of intelligence, Resnick L. B. (ed.), Erlbaum, Hillsdale, pp. 13-26.

2222. Usdin E., Mandell A.J. (eds.) (1978). Biochemistry of mental disorders, Dekker, New York, Basel.

2223. Valenstein E. S., Riss W., Young W. C. (1954). Sex drive in genetically heterogeneous and hughly inbred stains of male guinea pigs, J. Сотр. Physiol. Psychol., 47, 162-165.

2224. Valenstein E.S., Riss W, Young W.C. (1955). Experimental and genetic factors in the organization of sexual behavior in male guinea pigs, J. Сотр. Physiol. Psychol., 48, 397-403.

2225. Valverde F. (1967). Apical dendritic spines of the visual cortex and light deprivation in the mouse, Exp. Brain Res., 3, 337-352.

2226. Vandenberg S. G. (ed.) (1965). Methods and Goals in human Behavior Genetics, Academic Press, New York.


 

2227. Vandenberg S. G. (1968). Progress in human behavior genetics, Johns Hopkins Press, Baltimore.

2228. Vogel F. (1958). Über die Erblichkeit des normalen Elektroencephalogramms, Thieme, Stuttgart.

2229. Vogel F. (1981). Humangenetische Aspekte der Sucht, Dtsch. Med. Wschr., 106, 711-714.

2230. Vogel F. (1984). Mutation and selection in the marker (X) syndrome. A hypothesis, Ann. Hum. Genet, 48, 327-332.

2230a.Fo0e/ F., Kruger J., Hopp H. P., Schalt E., Schnabel R. (1986). Visually and auditory evoked EEG potentials in carriers of four hereditary EEG variants, Human Neurobiology, 5, 49-58.

2231. Vogel F., Schalt E. (1979). The electroencephalogram (EEG) as a research tool in human behavior genetics: Psychological examinations in healthy males with various inherited EEG variants. III. Interpretation of the results, Hum. Genet, 47, 81-111.

2232. Vogel F., Schalt E., Krüger J. (1979). The electroencephalogram (EEG) as a research tool in human behavior genetics: Psychological examinations in healthy males with various inherited EEG variants. II. Results, Hum. Genet, 47, 47-80.

2233. Vogel F., Schalt E., Krüger J., Klarich G. (1982). Relationship between behavioral maturation measured by the "Baum" test and EEG frequency. A pilot study on monozygotic and dizygotic twins, Hum. Genet, 62, 60-65.

2234. Vogel F., Schalt E., Krüger J., Propping P. (1979). The electroencephalogram (EEG) as a research tool in human behavior genetics: Psychological examinations in healthy males with various inherited EEG variants. I. Rationale of the study; material; methods; heritability of test parameters, Hum. Genet, 47, 1-45.

2234&.Volavka Jan, Mednick S. A., Rasmussen L., Sergeant J. (1977). EEG Spectra in XYY and XXY Men. Electroencephalography and Clinical Neurophysiology, 43, 798-801. Elsevier/ North-Holland, Scientific Publishers, Ltd.

2235. DeVriesJ.C., Vandenberg S.G., McClearn G.E. (1976). Genetics of specific cognitive abilities, Ann. Rev. Genet, 10, 179-207.

2236. Wahl O.P. (1976). Monozygotic twins discordant for schizophrenia: A review, Psychol. Bull., 83, 91-106.

2237. Wang J. C. C., Erbe R. W. (1984). Folate metabolism in cells from fragile X syndrome patients and carriers, Am. J. Med. Genet, 17, 303-310.

2238. Weinshilboum R.M. (1978). Human biochemical genetics of plasma dopamine-ß-hydroxilase and erythrocyte catechol-0-methyltransferase, Human genetic variation in response to medical and environmental agents: Pharmacogenetics and ecogenetics, Motulsky A. A. G. et al. (eds.), Hum. Genet, Suppl. 1, 101-111.

2239. Weinshilboum R.M. (1983). Biochemical genetics of catccholamincs in humans, Mayo Clin. Proc., 58, 319-330.


314 Литература


2240. Weinshilboum R. M., Schrott H. G., Raymond F. A., Weidman W. H., Elveback L. R. (1975). Inheritance of very low serum dopamine-ß-hydroxilase, Am. J. Hum. Genet, 27, 573-585.

2241. Wender P. H., Rosenthal D., Kety S.S. (1968). A psychiatric assessment of the adoptive parents of schizophrenics. In: The transmission of schizophrenia, Rosenthal D., Kety S. S. (eds.), Pergamon, Oxford, p. 235.

2242. Wender P. H., Rosenthal D., Kety S. S., Schulsinger E., Weiner J. (1976). Crosstesting. A research strategy for clarifying the role of genetic and environmental factors in the etiology of schizophrenia, Arch. Gen. Psychiatr., 30, 121.

2243. Williams R. J., Berry L. J., Beerstecher E. (1949). Biochemical individuality. III. Genetotrophic factors in the etiology of alcoholism, Arch. Biochem., 23, 275-290.

2244. Wilson R.S. (1972). Twins: Early mental development, Science, 175, 914-917.

2245. Winokur G., Tanna V.L. (1969). Possible role of X-linked dominant factor in manic-depressive disease, Dis. Nerv. Syst., 30, 89-94.

2246. Winter H., Herschel M., Propping P., Fried! W, Vogel F. (1978). A twin study on three enzymes (DBH, COMT, MAO) of Catecholamine metabolism, Psychopharmacology, 57, 63-69.

2247. Witkin H. A., Mednick S. A., Schulsinger F., Bakkestrtfm E., Christiansen К. 0., Goodenough D. R., Hirschhorn K., Lundsteen С., Owen D. R., Philip J., Rubin D. B., Stocking M. (1976). Criminality in XYY and XXY men, Science, 193, 547-555.

2248. Young W, Goy R.W., Phoenix C. H. (1964). Hormones and sexual behavior, Science, 143, 212-218.

2249. Zajonc R. B. (1976). Family configuration and intelligence, Science, 192, 227-236.

2250. ZangK.D. (ed.) (1984). Klinische Genetik des Alkoholismus, W. Kohlhammer Verlag, Stuttgart, Berlin, Köln, Mainz.

2251. Zerbin-Rüdin E. (1967). Idiopathischer Schwachsinn. In: Humangenetik, ein kurzes Handbuch, Becker P. E, (ed.), Vol. V/2, Thieme, Stuttgart, pp. 158-205.

2252. Zerbin-Rüdin E. (1957). Endogene Psychosen. In: Humangenetik, ein kurzes Handbuch, Becker P. E. (ed.), Band V/2, Thieme, Stuttgart, pp. 446-573.

Литература к главе 9 и приложению 8

2253. AdinolfiA., Adinolfl M., LessofM.H. (1975). Review: Alphafeto-protein during development and in disease, J. Med. Genet., 12, 138-151.

2254. Anonymous (1977). Methods for the detection of haemophilia carriers: a memorandum, WHO Bull., 55, 675-702.

2255. Anonymous (1975). Law and ethics of A.I.D. and embryo transfer, Ciba Found Symp. (new series), 17.


 

2256. Anonymous (1975). National Research Council. Committee for the Study of Inborn Errors of Metabolism. Genetic screening: programs, principles, and research, National Academy of Sciences, Washington (D.C.).

2257. Anonymous (1985). Embryo research, Lancet, 1, 255-256.

2258. Anonymous (1983). President's Commission for the Study of Ethical Problems in Medicine and Biomédical Research: Screening and Counseling for Genetic Conditions, The Ethical, Social, and Legal Implications of Genetic Screening, Counseling, and Education Program, US Government Printing Office, Washington, DC.

2259. Anonymous (1984). Report of the Committee on Inquiry into Human Fertilisation and Embryology, Her. Majesty's Stationery Office, London.

2260. Anonymous (1985). Maternal serum alpha-fetoprotein screening for neural tube defects. Results of a consensus meeting, Pren. Diag., 5, 77-83.

2261. Anonymous (1985). Low maternal serum alphafetoprotein and Down syndrome, Lancet, 1, 259-260.

2262. Applebaum E. G., Firestein S. К. (1983). А Genetic Conseling Casebook, The Free Press, New York.

2263. Bakker E., Hqfker M.H., Goor N., Mandel J.L., Wrogemann K., Davies K. E., Kunkel L. M., Willard H. F., Fenton W. A., Sandkuyl L., Majoor-Krakauer D., Essen A. J. V, Jahoda M. G. J., Sachs E. S., van Ommen G. J. B., Pearson P. L. (1985). Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs, Lancet, 1, 655-658.

2264. Berg P., Baltimore D., Boyer H. W., Cohen S. N., Davis R. W., Hogness D. S., Nathans D., Roblin R. O., Watson J. D., Weissman S., Zinder N.D. (1974). Potential biohazards of recombinant DNA molecules, Science, 185, 303.


Дата добавления: 2015-12-16 | Просмотры: 353 | Нарушение авторских прав







При использовании материала ссылка на сайт medlec.org обязательна! (0.028 сек.)