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High prevalence of RET/PTC rearrangements in Ukrainian and Belarussian post-chernobyl thyroid papillary carcinomas : A strong correlation between RET/PTC3 and the solid-follicular variant

The journal of clinical endocrinology and metabolism, 1999-11, Vol.84 (11), p.4232-4238

1999

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Gene rearrangement and Chernobyl related thyroid cancers

British journal of cancer, 2000-01, Vol.82 (2), p.315-322

2000

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Post-Chernobyl thyroid carcinoma in Belarus children and adolescents: Comparison with naturally occurring thyroid carcinoma in Italy and France

The journal of clinical endocrinology and metabolism, 1997-11, Vol.82 (11), p.3563-3569

1997

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The significance of the expression of matrix metalloproteinases in the differential diagnosis of periodontal diseases

Arkhiv patologii, 2021, Vol.83 (3), p.20

2021

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New breakpoints in both the H4 and RET genes create a variant of PTC‐1 in a post‐Chernobyl papillary thyroid carcinoma

Clinical endocrinology (Oxford), 2000-07, Vol.53 (1), p.131-136

2000

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High Prevalence of RET/PTC Rearrangements in Ukrainian and Belarussian Post-Chernobyl Thyroid Papillary Carcinomas: A Strong Correlation between RET/PTC3 and the Solid-Follicular Variant1

The journal of clinical endocrinology and metabolism, 1999-11, Vol.84 (11), p.4232-4238

1999

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The cerebro-reno-digital syndromes: a new community

Clinical genetics, 1991-02, Vol.39 (2), p.104-113

1991

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Renal agenesis as a diagnostic feature of the crypthophthalmos-syndactyly syndrome

Clinical genetics, 1984-06, Vol.25 (6), p.528-532

1984

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Difficulties in classification of the short rib-polydactyly syndromes

European journal of pediatrics, 1980, Vol.133 (1), p.57-61

1980

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Elaboration of the phenotypic changes of the upper limbs in the Neu-Laxova syndrome

American journal of medical genetics, 1985-01, Vol.20 (1), p.1-11

1985

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Campomelic syndrome: Concepts of the bowing and shortening in the lower limbs

Teratology (Philadelphia), 1987-02, Vol.35 (1), p.1-8

1987

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The Smith-Lemli-Opitz syndrome. A detailed pathological study as a clue to a etiological heterogeneity

Virchows Archiv A Pathological Anatomy and Histopathology, 1984-01, Vol.404 (4), p.413-425

1984

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The pathological anatomy of the Smith-Lemli-Opitz syndrome

Clinical genetics, 1975-05, Vol.7 (5), p.382-387

1975

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Renal agenesis as a diagnostic feature of the cryptophthalmos-syndactyly syndrome

Clinical genetics, 1984-06, Vol.25 (6), p.528-532

1984

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Pulmonary hypoplasia, multiple ankyloses, and camptodactyly: one syndrome or some related forms?

Helvetica paediatrica acta, 1978-04, Vol.33 (1), p.73

1978

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The XK-aprosencephaly syndrome

American journal of medical genetics, 1980, Vol.7 (2), p.231-234

1980

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The Wolf-Hirschhorn syndrome. II. Pathologic anatomy

Clinical genetics, 1980-07, Vol.18 (1), p.6-12

1980

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MORPHOLOGICAL AND IMMUNOHISTOCHEMICAL DESCRIPTION OF INTERSTITIAL TISSUE IN PRIMARY GLOMERULOPATHY

Health and Ecology Issues, 2009-06 (2), p.26-30

2009

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Further evidence for the autosomal-recessive inheritance of the COFS syndrome

Clinical genetics, 1976-12, Vol.10 (6), p.343-346

1976

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The popliteal pterygium syndrome (a condition of the main anatomical structures of the lower limbs)

Folia morphologica, 1983, Vol.31 (3), p.258

1983

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Brief clinical observations: the Neu-Laxova syndrome--a distinct entity

American journal of medical genetics, 1979, Vol.3 (3), p.261-267

1979

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A syndrome of multiple congenital malformations including amelia and oligodactyly occurring in half-cousins

Teratology (Philadelphia), 1976-04, Vol.13 (2), p.161-165

1976

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Further evidence'for the autosomal-recessive inheritance of the COFS syndrome

Clinical genetics, 1976-11, Vol.10 (5), p.343-346

1976

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The Wolf-Hirschhorn syndrome

Clinical genetics, 1980-07, Vol.18 (1), p.6-12

1980

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Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome

American journal of medical genetics, 1979, Vol.3 (3), p.301-309

1979

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High prevalence of RET/PTC rearrangements in Ukrainian and Belarussian post-chernobyl thyroid papillary carcinomas : A strong correlation between RET/PTC3 and the solid-follicular variant

Gene rearrangement and Chernobyl related thyroid cancers

Post-Chernobyl thyroid carcinoma in Belarus children and adolescents: Comparison with naturally occurring thyroid carcinoma in Italy and France

The significance of the expression of matrix metalloproteinases in the differential diagnosis of periodontal diseases

New breakpoints in both the H4 and RET genes create a variant of PTC‐1 in a post‐Chernobyl papillary thyroid carcinoma

High Prevalence of RET/PTC Rearrangements in Ukrainian and Belarussian Post-Chernobyl Thyroid Papillary Carcinomas: A Strong Correlation between RET/PTC3 and the Solid-Follicular Variant1

The cerebro-reno-digital syndromes: a new community

Renal agenesis as a diagnostic feature of the crypthophthalmos-syndactyly syndrome

Difficulties in classification of the short rib-polydactyly syndromes

Elaboration of the phenotypic changes of the upper limbs in the Neu-Laxova syndrome

Campomelic syndrome: Concepts of the bowing and shortening in the lower limbs

The Smith-Lemli-Opitz syndrome. A detailed pathological study as a clue to a etiological heterogeneity

The pathological anatomy of the Smith-Lemli-Opitz syndrome

Renal agenesis as a diagnostic feature of the cryptophthalmos-syndactyly syndrome

Pulmonary hypoplasia, multiple ankyloses, and camptodactyly: one syndrome or some related forms?

The XK-aprosencephaly syndrome

The Wolf-Hirschhorn syndrome. II. Pathologic anatomy

MORPHOLOGICAL AND IMMUNOHISTOCHEMICAL DESCRIPTION OF INTERSTITIAL TISSUE IN PRIMARY GLOMERULOPATHY

Further evidence for the autosomal-recessive inheritance of the COFS syndrome

The popliteal pterygium syndrome (a condition of the main anatomical structures of the lower limbs)

Brief clinical observations: the Neu-Laxova syndrome--a distinct entity

A syndrome of multiple congenital malformations including amelia and oligodactyly occurring in half-cousins

Further evidence'for the autosomal-recessive inheritance of the COFS syndrome

The Wolf-Hirschhorn syndrome

Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome

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