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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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Genetic Services in Israel

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

1997

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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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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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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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Further delineation of the acrocallosal syndrome

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

1991

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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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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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Carcinoma of pancreas associated with the 5q-syndrome

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

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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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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Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

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

1985

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14 years follow-up in a patient with Fanconi anemia. Clinical, haematological and cytogenetical study

Haematologica (Roma), 1979-08, Vol.64 (4), p.472

1979

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The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+)

Journal of medical genetics, 1971-09, Vol.8 (3), p.346-350

1971

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Testicular feminisation syndrome: unusual gonadal histology in an elderly patient

Journal of medical genetics, 1977-10, Vol.14 (5), p.375-378

1977

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Multiple skeletal anomalies in the "13q-" syndrome

European journal of pediatrics, 1978-05, Vol.128 (1), p.27-31

1978

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Pure trisomy 17p in 60% cells

Human genetics, 1979, Vol.52 (3), p.263-268

1979

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Absent ulna in the Klippel-Feil syndrome: an unusual associated malformation

Clinical genetics, 1980-02, Vol.17 (2), p.167-170

1980

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Myeloproliferative disease of childhood associated with a trisomy 21 clone

Acta haematologica, 1979-01, Vol.62 (2), p.90-93

1979

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Epidermal mosaicism and Blaschko's lines

Genetic Services in Israel

Medical genetics in Israel

Teratogenicity of progestogens given during the first trimester of pregnancy

Aberrant melanoblast migration associated with trisomy 18 mosaicism

Further delineation of the acrocallosal syndrome

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

Chorionic villus sampling for fetal karyotyping in missed abortions

Cryptophthalmus syndrome without cryptophthalmus

CHROMOSOMAL ABNORMALITIES IN SEZARY'S LYMPHOMA

Familial macroglossia-omphalocele syndrome

Carcinoma of pancreas associated with the 5q-syndrome

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

Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

14 years follow-up in a patient with Fanconi anemia. Clinical, haematological and cytogenetical study

The inheritance of a structural anomaly of one chromosome No. 16 in a kindred (46,16-,C+)

Testicular feminisation syndrome: unusual gonadal histology in an elderly patient

Multiple skeletal anomalies in the "13q-" syndrome

Pure trisomy 17p in 60% cells

Absent ulna in the Klippel-Feil syndrome: an unusual associated malformation

Myeloproliferative disease of childhood associated with a trisomy 21 clone

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