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Genetic Services in Israel

European journal of human genetics : EJHG, 1997-01, Vol.5 (Suppl 2), p.105-111

1997

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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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CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES: A COMPARATIVE STUDY

Prenatal diagnosis, 1996-02, Vol.16 (2), p.165-168

1996

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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

1985

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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, 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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3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

Journal of inherited metabolic disease, 1992-01, Vol.15 (2), p.204-212

1992

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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.331-332

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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The dilemma of chromosomal mosaicism in chorionic villus sampling-'direct' versus long-term cultures

Prenatal diagnosis, 1989-04, Vol.9 (4), p.223-226

1989

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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.343-345

1984

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Trisomy 9 confined to the placenta: Prenatal diagnosis and neonatal follow-up

American journal of medical genetics, 1991-09, Vol.40 (4), p.464-466

1991

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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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Cystic fibrosis: linked DNA markers in prenatal diagnosis and carrier detection

הרפואה, 1988-04, Vol.114 (7), p.317

1988

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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.66-67

1983

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Familial recurring thanatophoric dwarfism. A case report

Obstetrics and gynecology (New York. 1953), 1972-04, Vol.39 (4), p.515

1972

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Genetic Services in Israel

Pelvis-shoulder dysplasia

Medical genetics in Israel

CYTOGENETIC ANALYSIS OF FETAL CHONDROCYTES: A COMPARATIVE STUDY

Teratogenicity of progestogens given during the first trimester of pregnancy

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)

3‐Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’)

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

The dilemma of chromosomal mosaicism in chorionic villus sampling-'direct' versus long-term cultures

Carcinoma of pancreas associated with the 5q-syndrome

Weissenbacher-Zweymüller syndrome: A distinct autosomal recessive skeletal dysplasia

Philadelphia chromosome in idiopathic acquired sideroblastic anemia

Trisomy 9 confined to the placenta: Prenatal diagnosis and neonatal follow-up

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

Cystic fibrosis: linked DNA markers in prenatal diagnosis and carrier detection

Male to male transmission of the G syndrome

Cytogenetic studies in megakaryoblastic leukaemia

Familial recurring thanatophoric dwarfism. A case report

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