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Epidermal mosaicism and Blaschko's lines

Journal of medical genetics, 1994-03, Vol.31 (3), p.260-260

Chemke, J

1994

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Pelvis-shoulder dysplasia

Pediatric radiology, 1998-09, Vol.28 (9), p.681-682

1998

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Medical genetics in Israel

European journal of human genetics : EJHG, 1995, Vol.3 (3), p.147-154

1995

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Autosomal recessive inheritance of Nager acrofacial dysostosis

Journal of medical genetics, 1988-04, Vol.25 (4), p.230-232

1988

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Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

Obstetrics and gynecology (New York. 1953), 1985-06, Vol.65 (6), p.775-780

1985

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Aberrant melanoblast migration associated with trisomy 18 mosaicism

Journal of medical genetics, 1983-04, Vol.20 (2), p.135-137

1983

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COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: Molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED)

American journal of medical genetics. Part A, 2005-01, Vol.132A (1), p.33-35

2005

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Further delineation of the acrocallosal syndrome

European journal of pediatrics, 1991-09, Vol.150 (11), p.797-799

1991

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Homozygosity for inversion (2)(q12q14)

Human genetics, 1993-10, Vol.92 (4), p.427-427

1993

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Isolated foveal hypoplasia

British journal of ophthalmology, 1987-12, Vol.71 (12), p.926-930

1987

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Occurrence of hereditary nephritis, pretibial epidermolysis bullosa and beta-thalassemia minor in two siblings with end-stage renal disease

Nephron (2015), 1988, Vol.49 (4), p.331

1988

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Prenatal diagnosis of genetic diseases

Israel journal of medical sciences, 1986-03, Vol.22 (3-4), p.207

Chemke, J

1986

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Chorionic villus sampling for fetal karyotyping in missed abortions

Prenatal diagnosis, 1991-01, Vol.11 (1), p.55-57

1991

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Cryptophthalmus syndrome without cryptophthalmus

The Journal of clinical dysmorphology, 1983-06, Vol.1 (2), p.31

Chemke, J

1983

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CHROMOSOMAL ABNORMALITIES IN SEZARY'S LYMPHOMA

European journal of haematology, 1989-07, Vol.43 (1), p.85-85

1989

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Familial macroglossia-omphalocele syndrome

Journal de genetique humaine, 1976-12, Vol.24 (4), p.271

Chemke, J

1976

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Familial café au lait spots: a variant of neurofibromatosis type 1

Journal of medical genetics, 1995-12, Vol.32 (12), p.985-986

1995

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Carcinoma of pancreas associated with the 5q-syndrome

Anticancer research, 1984-05, Vol.4 (3), p.205

1984

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Weissenbacher-Zweymüller syndrome: A distinct autosomal recessive skeletal dysplasia

American journal of medical genetics, 1992-08, Vol.43 (6), p.989-995

1992

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Philadelphia chromosome in idiopathic acquired sideroblastic anemia

Acta haematologica, 1984-01, Vol.72 (5), p.343

1984

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Down's syndrome: denial of infant rights and the chance to live

הרפואה, 1986-08, Vol.111 (3-4), p.67

1986

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Homozygosity for autosomal dominant Marfan syndrome

Journal of medical genetics, 1984-06, Vol.21 (3), p.173-177

1984

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Male to male transmission of the G syndrome

Clinical genetics, 1984-08, Vol.26 (2), p.164-164

1984

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Cytogenetic studies in megakaryoblastic leukaemia

Acta haematologica, 1983, Vol.69 (1), p.66

1983

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Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

Obstetrical & gynecological survey, 1985-11, Vol.40 (11), p.697-698

1985

Volltextzugriff (PDF)

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Epidermal mosaicism and Blaschko's lines

Pelvis-shoulder dysplasia

Medical genetics in Israel

Autosomal recessive inheritance of Nager acrofacial dysostosis

Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

Aberrant melanoblast migration associated with trisomy 18 mosaicism

COL11A2 mutation associated with autosomal recessive Weissenbacher-Zweymuller syndrome: Molecular and clinical overlap with otospondylomegaepiphyseal dysplasia (OSMED)

Further delineation of the acrocallosal syndrome

Homozygosity for inversion (2)(q12q14)

Isolated foveal hypoplasia

Occurrence of hereditary nephritis, pretibial epidermolysis bullosa and beta-thalassemia minor in two siblings with end-stage renal disease

Prenatal diagnosis of genetic diseases

Chorionic villus sampling for fetal karyotyping in missed abortions

Cryptophthalmus syndrome without cryptophthalmus

CHROMOSOMAL ABNORMALITIES IN SEZARY'S LYMPHOMA

Familial macroglossia-omphalocele syndrome

Familial café au lait spots: a variant of neurofibromatosis type 1

Carcinoma of pancreas associated with the 5q-syndrome

Weissenbacher-Zweymüller syndrome: A distinct autosomal recessive skeletal dysplasia

Philadelphia chromosome in idiopathic acquired sideroblastic anemia

Down's syndrome: denial of infant rights and the chance to live

Homozygosity for autosomal dominant Marfan syndrome

Male to male transmission of the G syndrome

Cytogenetic studies in megakaryoblastic leukaemia

Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

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