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High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect

Human mutation, 1998, Vol.11 (S1), p.S53-S54

1998

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Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia

Human mutation, 1995, Vol.5 (2), p.131-136

1995

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Uterine Artery Embolization as Nonsurgical Treatment of Uterine Myomas

ISRN obstetrics and gynecology, 2011-01, Vol.2011 (2011), p.1-4

2011

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An uncommon phenotypical variant in the Shereshevsky-Turner syndrome

Human genetics, 1979-01, Vol.52 (3), p.275-279

1979

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High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect

Human mutation, 1998, Vol.Suppl 1, p.S53-S54

1998

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Structural rearrangement of chromosome 1 and 46, XY-47, XXY mosaicism in a child with a disorder of sex differentiation

Soviet genetics, 1974-07, Vol.8 (7), p.932

1974

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Stereotaxic cryosurgery in patients with Parkinson's disease. Long-term results

Clinical neurology and neurosurgery, 1997-07, Vol.99, p.S160-S160

1997

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Methods for obtaining fetal blood and its characterization

Akusherstvo i ginekologii͡a, 1994 (1), p.21

1994

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Diagnosis of heterozygote carrier of mutant gene of 21-hydroxylase

Akusherstvo i ginekologii͡a, 1995 (1), p.21

1995

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Typical form of gonadal dysgenesis (etiology, clinical aspects, treatment)

Meditsinskaia sestra, 1983-08, Vol.42 (8), p.15

Dzenis, I G

1983

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Clinico-genealogic analysis of different forms of hypogonadism in girls

Akusherstvo i ginekologii͡a, 1985-11 (11), p.11

1985

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Clinical variants of virile form of congenital adrenocortical dysfunction

Akusherstvo i ginekologii͡a, 1990-04 (4), p.25

1990

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Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype

Akusherstvo i ginekologii͡a, 1990-01 (1), p.10

1990

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The steroid content of the amniotic fluid in the 1st and 2nd pregnancy trimesters in 21-hydroxylase insufficiency and in fetal central nervous system defects

Akusherstvo i ginekologii͡a, 1995 (2), p.23

1995

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Congenital dysfunction of adrenal cortex - detection of new mutant gene of 21-hydroxylase

Vestnik Rossiĭskoĭ akademii medits︠i︡nskih nauk, 1994 (12), p.29

1994

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Features of adrenal cortex function in heterozygous carriers of 21-hydroxylase deficiency

Problemy ėndokrinologii, 1991-01, Vol.37 (1), p.34

1991

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The functional characteristics of the reproductive system in women who are heterozygous carriers of 21-hydroxylase deficiency

Akusherstvo i ginekologii͡a, 1990-09 (9), p.49

1990

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Diagnosis of the diseases accompanying retardation of sexual development

Akusherstvo i ginekologii͡a, 1979-07 (7), p.56

1979

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Hermaphroditism: its pathogenesis, clinical picture and the means of therapy

Akusherstvo i ginekologii͡a, 1978-08 (8), p.67

1978

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Gonadal dysgenesis

Akusherstvo i ginekologii͡a, 1977-02 (2), p.67

1977

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Longitudinal differentiation of human mitotic chromosomes. Communication II. Analysis of pericentric inversion of the first chromosome in a child with anomalous sex differentiation

Soviet genetics, 1974-07, Vol.8 (6), p.770

1974

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Comparative analysis of the karyotype and phenotype of girls lacking signs of sexual development

TSitologiia i genetika, 1977-01, Vol.11 (1), p.13

1977

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State of permanent teeth in mixed forms of gonadal dysgenesis

Stomatologija (Moskva), 1976-05, Vol.55 (3), p.90

1976

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Testicular feminization syndrome in children

Problemy ėndokrinologii, 1976-11, Vol.22 (6), p.29

1976

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Chromosomal polymorphism in patients with ovarian hypofunction of central origin

TSitologiia i genetika, 1984-03, Vol.18 (2), p.144

1984

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High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect

Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia

Uterine Artery Embolization as Nonsurgical Treatment of Uterine Myomas

An uncommon phenotypical variant in the Shereshevsky-Turner syndrome

High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect

Structural rearrangement of chromosome 1 and 46, XY-47, XXY mosaicism in a child with a disorder of sex differentiation

Stereotaxic cryosurgery in patients with Parkinson's disease. Long-term results

Methods for obtaining fetal blood and its characterization

Diagnosis of heterozygote carrier of mutant gene of 21-hydroxylase

Typical form of gonadal dysgenesis (etiology, clinical aspects, treatment)

Clinico-genealogic analysis of different forms of hypogonadism in girls

Clinical variants of virile form of congenital adrenocortical dysfunction

Clinical polymorphism of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency and HLA phenotype

The steroid content of the amniotic fluid in the 1st and 2nd pregnancy trimesters in 21-hydroxylase insufficiency and in fetal central nervous system defects

Congenital dysfunction of adrenal cortex - detection of new mutant gene of 21-hydroxylase

Features of adrenal cortex function in heterozygous carriers of 21-hydroxylase deficiency

The functional characteristics of the reproductive system in women who are heterozygous carriers of 21-hydroxylase deficiency

Diagnosis of the diseases accompanying retardation of sexual development

Hermaphroditism: its pathogenesis, clinical picture and the means of therapy

Gonadal dysgenesis

Longitudinal differentiation of human mitotic chromosomes. Communication II. Analysis of pericentric inversion of the first chromosome in a child with anomalous sex differentiation

Comparative analysis of the karyotype and phenotype of girls lacking signs of sexual development

State of permanent teeth in mixed forms of gonadal dysgenesis

Testicular feminization syndrome in children

Chromosomal polymorphism in patients with ovarian hypofunction of central origin

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