UB Paderborn / Katalog / Suche / in CDI

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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Homozygosity for autosomal dominant Marfan syndrome

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

1984

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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

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

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Familial Recurring Thanatophoric Dwarfism: A Case Report

Obstetrics and gynecology (New York. 1953), 1972-04, Vol.39 (4), p.515-520

1972

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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

1979

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Prenatal diagnosis of SLO syndrome

American journal of medical genetics, 1995-04, Vol.56 (3), p.288-288

1995

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Occurrence of four types of growth hormone-related dwarfism in Israeli communities

European journal of pediatrics, 1981-09, Vol.137 (1), p.35-39

1981

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BISATELLITED MICROCHROMOSOMES AND MULTIPLE CONGENITAL MALFORMATIONS

Acta Paediatrica, 1983-05, Vol.72 (3), p.469-471

1983

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Familial glioblastoma multiforme without neurofibromatosis

American journal of medical genetics, 1985-08, Vol.21 (4), p.731-735

1985

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ABSENCE OF CHROMOSOMAL CHANGES IN FETUS AFTER PATERNAL CHEMOTHERAPY

The Lancet (British edition), 1979-09, Vol.314 (8143), p.637-637

1979

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Antenatal Ultrasonic Diagnosis of Complete Urethral Obstruction in the Fetus

Acta obstetricia et gynecologica Scandinavica, 1980, Vol.59 (5), p.463-465

1980

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Prenatal diagnosis of severe congenital malformations associated with elevated amniotic fluid alpha-feto protein

Clinical genetics, 1979-04, Vol.15 (4), p.351-355

1979

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Familial Down's syndrome

Journal de genetique humaine, 1977-10, Vol.25 (3), p.189

1977

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Maple syrup urine disease. Two cases in Israel

Israel journal of medical sciences, 1975-08, Vol.11 (8), p.809

1975

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Ethnic distribution of the fragile X syndrome in Israel: evidence of founder chromosomes(?)

Israel journal of medical sciences, 1995-05, Vol.31 (5), p.323

1995

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

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

Homozygosity for autosomal dominant Marfan syndrome

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

Male to male transmission of the G syndrome

Cytogenetic studies in megakaryoblastic leukaemia

Teratogenicity of Progestogens Given During the First Trimester of Pregnancy

Familial Recurring Thanatophoric Dwarfism: A Case Report

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

Prenatal diagnosis of SLO syndrome

Occurrence of four types of growth hormone-related dwarfism in Israeli communities

BISATELLITED MICROCHROMOSOMES AND MULTIPLE CONGENITAL MALFORMATIONS

Familial glioblastoma multiforme without neurofibromatosis

ABSENCE OF CHROMOSOMAL CHANGES IN FETUS AFTER PATERNAL CHEMOTHERAPY

Antenatal Ultrasonic Diagnosis of Complete Urethral Obstruction in the Fetus

Prenatal diagnosis of severe congenital malformations associated with elevated amniotic fluid alpha-feto protein

Familial Down's syndrome

Maple syrup urine disease. Two cases in Israel

Ethnic distribution of the fragile X syndrome in Israel: evidence of founder chromosomes(?)

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