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The genetics of familial cases of diaphragmatic hernia

TSitologiia i genetika, 1988-03, Vol.22 (2), p.67

1988

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Indications for amniocentesis for prenatal determination of fetal karyotype

TSitologiia i genetika, 1976-05, Vol.10 (3), p.198

Lur'e, I V

1976

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Simpson's syndrome and Golabi-Rosen syndrome: the same disease or 2 different but close forms?

Pediatrija, 1987 (6), p.81

1987

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The importance of medico-genetic services in the prophylaxis of disability in children

Pediatrija, 1991 (6), p.66

1991

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Genetics of congenital esophageal defects

TSitologiia i genetika, 1984-11, Vol.18 (6), p.463

1984

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Congenital developmental defects in the genetic monitoring system. I. The selection of developmental defects subject to dynamic observation

Genetika, 1983, Vol.19 (1), p.165

1983

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Some ideas on the time sequence of chromosome function in human organogenesis

Soviet genetics, 1974-07, Vol.8 (6), p.774

Lur'e, I V

1974

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Influence of parental age on "de novo" translocations

Soviet genetics, 1974-05, Vol.8 (3), p.399

Lur'e, I V

1974

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Analysis of phenotypic variability of Zimmermann-Laband syndrome

Pediatrija, 1988 (4), p.86

1988

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Translocation 11q;22q: a clinico-cytogenetic study

Genetika, 1992-10, Vol.28 (10), p.129

1992

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Smith-Lemli-Opitz syndrome: evaluation of the correlations between individual traits as an approach to the study of heterogeneity

TSitologiia i genetika, 1987-01, Vol.21 (1), p.57

1987

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Genetics of partial trisomies. Trisomy 4p

Genetika, 1989-03, Vol.25 (3), p.565

1989

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"Teratologic series" and their genetics

Genetika, 1979, Vol.15 (5), p.912

1979

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Treatment of light-induced hyperpigmentation of the skin with hydroquinone monobenzyl ester

Vestnik dermatologij i venerologij, 1968-02, Vol.42 (2), p.84

1968

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Genetics of partial trisomies. I. Trisomy 2q

Genetika, 1986-06, Vol.22 (6), p.1033

1986

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Van der Hoeve's syndrome

Klinicheskaia meditsina, 1969-03, Vol.47 (3), p.143

1969

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Eye anomalies in chromosomal aberrations

Oftalmologicheskii zhurnal, 1971, Vol.26 (4), p.299

1971

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Trisomy for distal segments of the long arm of chromosome 1

Genetika, 1989-12, Vol.25 (12), p.2251

1989

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Genetic syndromes of multiple congenital developmental defects

Arkhiv patologii, 1977, Vol.39 (3), p.3

1977

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Genetic characteristics of the "EEC" syndrome (ectrodactyly, ectodermal dysplasis, cheilognathopalatoschisis)

Genetika, 1976, Vol.12 (7), p.125

1976

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Pathological anatomy of monogenic syndromes of multiple congenital developmental defects

Arkhiv patologii, 1984, Vol.46 (4), p.39

1984

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Arrhinencephaly in aberrations of autosomal chromosomes and sequential chromosomal functional expression

Soviet genetics, 1973-07, Vol.7 (1), p.123

1973

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Prenatal diagnosis of fetal developmental defects from anamnestic findings and the course of pregnancy

Akusherstvo i ginekologii͡a, 1976-11 (11), p.58

1976

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Langer-Giedion syndrome and deletion in the long arm of chromosome 8

Genetika, 1987-05, Vol.23 (5), p.907

1987

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Genetic counseling in cases of chromosome insertions

Genetika, 1975, Vol.11 (9), p.131

1975

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The genetics of familial cases of diaphragmatic hernia

Indications for amniocentesis for prenatal determination of fetal karyotype

Simpson's syndrome and Golabi-Rosen syndrome: the same disease or 2 different but close forms?

The importance of medico-genetic services in the prophylaxis of disability in children

Genetics of congenital esophageal defects

Congenital developmental defects in the genetic monitoring system. I. The selection of developmental defects subject to dynamic observation

Some ideas on the time sequence of chromosome function in human organogenesis

Influence of parental age on "de novo" translocations

Analysis of phenotypic variability of Zimmermann-Laband syndrome

Translocation 11q;22q: a clinico-cytogenetic study

Smith-Lemli-Opitz syndrome: evaluation of the correlations between individual traits as an approach to the study of heterogeneity

Genetics of partial trisomies. Trisomy 4p

"Teratologic series" and their genetics

Treatment of light-induced hyperpigmentation of the skin with hydroquinone monobenzyl ester

Genetics of partial trisomies. I. Trisomy 2q

Van der Hoeve's syndrome

Eye anomalies in chromosomal aberrations

Trisomy for distal segments of the long arm of chromosome 1

Genetic syndromes of multiple congenital developmental defects

Genetic characteristics of the "EEC" syndrome (ectrodactyly, ectodermal dysplasis, cheilognathopalatoschisis)

Pathological anatomy of monogenic syndromes of multiple congenital developmental defects

Arrhinencephaly in aberrations of autosomal chromosomes and sequential chromosomal functional expression

Prenatal diagnosis of fetal developmental defects from anamnestic findings and the course of pregnancy

Langer-Giedion syndrome and deletion in the long arm of chromosome 8

Genetic counseling in cases of chromosome insertions

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