Published in Vestn Akad Med Nauk SSSR on January 01, 1973
[The frequency of X-linked mental retardation]. Genetika (1989) 0.97
[A schizophrenia-like variant of phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova (1975) 0.76
[Obstetrical problems of phenylketonuria]. Akush Ginekol (Mosk) (1976) 0.75
[Heterochromatic regions of human chromosomes 1, 9, 16 and Y and the phenotype]. Genetika (1984) 0.75
[Medico-genetic consultation in monosymptomatic sensorineural deafness]. Vestn Otorinolaringol (1985) 0.75
[Children with ring chromosome 13]. Pediatriia (1981) 0.75
[Incidence of oligophrenia with fragile X chromosome (FraXq27)]. Genetika (1987) 0.75
[Clinical and electroencephalographic features of the convulsive syndrome in phenylketonuria in children]. Zh Nevropatol Psikhiatr Im S S Korsakova (1969) 0.75
[Malignant forms of phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova (1984) 0.75
[On the pathogenesis of the neuropsychiatric sequelae of ABO incompatibility between mother and fetus]. Zh Nevropatol Psikhiatr Im S S Korsakova (1968) 0.75
[Characteristics of medical genetic counseling in hearing disorders]. Vestn Otorinolaringol (1982) 0.75
[A simplified method of determining the serum concentration of phenylalanine]. Lab Delo (1972) 0.75
[Genetic study of sensorineural hearing loss]. Genetika (1982) 0.75
[On the incidence of psychic disturbances in children born from immunologically incompatible (ABO factors) pregnancy]. Zh Nevropatol Psikhiatr Im S S Korsakova (1965) 0.75
[Analysis of some genotypic and environmental causes for the early onset of schizophrenia]. Zh Nevropatol Psikhiatr Im S S Korsakova (1974) 0.75
[Clinical manifestations of oligophrenia with fragile X syndrome in boys in the pre- and post-pubertal age]. Zh Nevropatol Psikhiatr Im S S Korsakova (1989) 0.75
[About probable causes of early manifestation of schizophrenia (author's transl)]. Cesk Psychiatr (1975) 0.75
[Frequency and types of inheritance of genetic neurosensory hearing loss in children]. Vestn Otorinolaringol (1981) 0.75
[Families with recurrent cases of Waardenburg-Klein syndrome]. Genetika (1985) 0.75
[On the dynamics of psychopathologic manifestations in phenylketonuria (phenylpyruvic oligophrenia)]. Zh Nevropatol Psikhiatr Im S S Korsakova (1967) 0.75
[Polymorphism of clinical manifestations and characteristics of imbecility in the Laurence-Moon-Biedl syndrome]. Zh Nevropatol Psikhiatr Im S S Korsakova (1989) 0.75
[Medico-genetic consultation for families with neurosensory hypoacusis of unknown etiology in both spouses]. Vestn Otorinolaringol (1987) 0.75
[Clinico-electroencephalographic evaluation of the effectiveness of diet therapy in patients with phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova (1972) 0.75
[Pressing problems of phenylketonuria]. Pediatriia (1980) 0.75
[Genetic characteristics of recessive sensorineural hearing loss]. Genetika (1987) 0.75
[Constitution and psychoses (body build and psychoses) (review of the literature)]. Zh Nevropatol Psikhiatr Im S S Korsakova (1973) 0.75
[Genetic forms of rapidly progressive neurosensory hearing loss]. Vestn Otorinolaringol (1986) 0.75
[Experience with treatment of children with phenylketonuria]. Zh Nevropatol Psikhiatr Im S S Korsakova (1969) 0.75
[Classification of hereditary sensorineural deafness]. Vestn Otorinolaringol (1986) 0.75
Medical genetic study of the population of the western Pamir. I. Sex ratio, hereditary neuropsychiatric diseases, and general anthropogenetic traits. Sov Genet (1971) 0.75
[The intellectual defect in phenylketonuria, its dynamics and structure]. Zh Nevropatol Psikhiatr Im S S Korsakova (1972) 0.75
[Polymorphism of the heterochromatic regions of chromosomes 1, 9, 16 and Y and mental retardation]. Genetika (1984) 0.75
[Etiology of neurosensory hearing loss in children with normal-hearing parents]. Vestn Otorinolaringol (1982) 0.75
[Autosomal anomalies in a specially selected group of children with mental retardation without signs of Down's syndrome]. Zh Nevropatol Psikhiatr Im S S Korsakova (1982) 0.75
[Phenylalanine level in the serum of heterozygotes for phenylketonuria under intensified protein catabolism]. Genetika (1981) 0.75
[Phenylketonuria with congenital megaloblastic anemia]. Pediatriia (1981) 0.75
[Problem of the clinical aspects and treatment of phenylketonuria in children]. Vopr Okhr Materin Det (1969) 0.75
[Basic principles for the organisation of medical genetic care of the population]. Z Arztl Fortbild (Jena) (1972) 0.75
[Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children]. Vestn Otorinolaringol (1980) 0.75
[A supposed deletion in the long arm of one of the group B chromosomes in a peculiar form of oligophrenia]. Tsitologiia (1968) 0.75
[Multiple birth and Down's disease]. Genetika (1975) 0.75
[Clinical polymorphism of the Waardenburg-Klein syndrome in children]. Pediatriia (1987) 0.75
[Differential approach to genetic prognosis for progeny in cases of sporadic sensorineural deafness in children]. Vestn Otorinolaringol (1983) 0.75
[Constitution and psychoses (mental and psychopathic constitutions and psychoses) (a review of the literature)]. Zh Nevropatol Psikhiatr Im S S Korsakova (1973) 0.75
[Relationship between the severity of brain damage in phenylketonuria and the degree of hyperphenylalaninemia]. Zh Nevropatol Psikhiatr Im S S Korsakova (1980) 0.75
[Effect of maternal genetic heterozygosity]. Genetika (1975) 0.75
[A medico-genetic study of the population of Western Pamir. IV, Several hereditary neuropsychiatric diseases among the population of the Bartang canyon]. Genetika (1976) 0.75
[Spontaneous abortions in women-carriers of the phenylketonuria gene]. Akush Ginekol (Mosk) (1972) 0.75
[Syndrome of supravalvular aortic stenosis in children]. Pediatriia (1984) 0.75
Medical-genetic study of the population of the Western Pamir. II. Hemoglobins and ABO, MN, Rh, P, and Le blood groups. Sov Genet (1974) 0.75
[State of nuclear chromatin of peripheral blood lymphocytes in Down's syndrome and phenylketonuria detected by a cytospectrofluorometric method]. Biull Eksp Biol Med (1971) 0.75
[Heterochromatic regions of chromosomes 1, 9, 16 and Y in children with signs of embryonic development disorder]. Genetika (1982) 0.75
[New form of dominant hereditary neurosensory hearing loss]. Vestn Otorinolaringol (1982) 0.75