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An association between low maternal serum α-fetoprotein and fetal chromosomal abnormalities

American journal of obstetrics and gynecology, 1984-04, Vol.148 (7), p.886-894

1984

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Potential mapping of corneal dermoids to Xq24-qter

Journal of medical genetics, 2001-10, Vol.38 (10), p.719-723

2001

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The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal gland

Pediatric research, 1982-03, Vol.16 (3), p.172-175

1982

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Genetic Polymorphism (G80A) of Reduced Folate Carrier Gene in Ethnic Populations

Molecular genetics and metabolism, 2001-07, Vol.73 (3), p.285-286

2001

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Procedure-related fetal losses in transplacental versus nontransplacental genetic amniocentesis

American journal of obstetrics and gynecology, 1995-03, Vol.172 (3), p.868-872

1995

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Pregnancy outcome in women with sickle cell trait

JAMA : the journal of the American Medical Association, 1977-09, Vol.238 (13), p.1392

1977

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PREGNANCY OUTCOME IN WOMEN WITH SICKLE CELL TRAIT

Obstetrical & gynecological survey, 1978-05, Vol.33 (5), p.330-331

1978

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GENETIC COUNSELING: OBJECTIVES, PRINCIPLES AND PROCEDURES

Clinical obstetrics and gynecology, 1976-12, Vol.19 (4), p.919-940

Nitowsky, Harold M

1976

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Methylenetetrahydrofolate Reductase (MTHFR): High Incidence of Mutation C677T in Ashkenazi Jewish Population

Pediatric research, 1999-04, Vol.45 (4, Part 2 of 2), p.140-140A

1999

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Alkaline Phosphatase in Cell Cultures of Human Origin

Nature (London), 1961-03, Vol.189 (4766), p.756-757

1961

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Quinacrine Mustard Fluorescence of Sex Chromatin in Human Amniotic Fluid Cell Cultures

Nature (London), 1972-01, Vol.235 (5335), p.226-229

1972

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Altered lysosomal glycohydrolase activities in juvenile diabetes mellitus

Diabetes (New York, N.Y.), 1976-05, Vol.25 (5), p.420-427

1976

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Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A

American journal of medical genetics, 2002-01, Vol.107 (2), p.162-168

2002

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Early amniocentesis versus chorionic villus sampling for fetal karyotyping

The Lancet (British edition), 1994-09, Vol.344 (8925), p.825-826

1994

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Skin Biopsy for Cell Culture

Nature (London), 1963-07, Vol.199 (4890), p.296-297

1963

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Further delineation of the McKusick-Kaufman hydrometrocolpos-polydactyly syndrome

American journal of diseases of children (1960), 1987-10, Vol.141 (10), p.1133

1987

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Demonstration of Two Populations of Cells in the Human Female Heterozygous for Glucose-6-phosphate Dehydrogenase Variants

Proceedings of the National Academy of Sciences - PNAS, 1963-09, Vol.50 (3), p.481-485

1963

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Characterization of Three Overlapping Deletions Causing X-Linked Lymphoproliferative Disease

Genomics (San Diego, Calif.), 1993-04, Vol.16 (1), p.254-255

1993

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Early detection of abdominal pregnancy by maternal serum AFP+ screening

Prenatal diagnosis, 1994-12, Vol.14 (12), p.1155-1157

1994

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Studies of Jocopherol Deficiency in Infants and Children: II. Plasma Tocopherol and Erythrocyte Hemolysis in Hydrogen Peroxide

A.M.A. journal of diseases of children, 1956-08, Vol.92 (2), p.164

NITOWSKY, HAROLD M.

1956

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Abortion and ethics: making informed decisions

Conservative Judaism, 1975, Vol.29 (4), p.26

Nitowsky, Harold

1975

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Studies of tocopherol deficiency in infants and children. I. Hemolysis of erythrocytes in hydrogen peroxide

A.M.A. American journal of diseases of children, 1955-12, Vol.90 (6), p.669

1955

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Effect of hemopoietic and other agents on the hydroxyphenyluria of premature infants

A.M.A. American journal of diseases of children, 1953-04, Vol.85 (4), p.462

1953

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FEASIBILITY OF FRAGILE X CHROMOSOME PRENATAL DIAGNOSIS DEMONSTRATED

The Lancet (British edition), 1981-12, Vol.318 (8258), p.1292-1292

1981

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Split hand and foot deformity and the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC): A report of five patients

Human genetics, 1977, Vol.39 (1), p.15-25

1977

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An association between low maternal serum α-fetoprotein and fetal chromosomal abnormalities

Potential mapping of corneal dermoids to Xq24-qter

The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal gland

Genetic Polymorphism (G80A) of Reduced Folate Carrier Gene in Ethnic Populations

Procedure-related fetal losses in transplacental versus nontransplacental genetic amniocentesis

Pregnancy outcome in women with sickle cell trait

PREGNANCY OUTCOME IN WOMEN WITH SICKLE CELL TRAIT

GENETIC COUNSELING: OBJECTIVES, PRINCIPLES AND PROCEDURES

Methylenetetrahydrofolate Reductase (MTHFR): High Incidence of Mutation C677T in Ashkenazi Jewish Population

Alkaline Phosphatase in Cell Cultures of Human Origin

Quinacrine Mustard Fluorescence of Sex Chromatin in Human Amniotic Fluid Cell Cultures

Altered lysosomal glycohydrolase activities in juvenile diabetes mellitus

Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A

Early amniocentesis versus chorionic villus sampling for fetal karyotyping

Skin Biopsy for Cell Culture

Further delineation of the McKusick-Kaufman hydrometrocolpos-polydactyly syndrome

Demonstration of Two Populations of Cells in the Human Female Heterozygous for Glucose-6-phosphate Dehydrogenase Variants

Characterization of Three Overlapping Deletions Causing X-Linked Lymphoproliferative Disease

Early detection of abdominal pregnancy by maternal serum AFP+ screening

Studies of Jocopherol Deficiency in Infants and Children: II. Plasma Tocopherol and Erythrocyte Hemolysis in Hydrogen Peroxide

Abortion and ethics: making informed decisions

Studies of tocopherol deficiency in infants and children. I. Hemolysis of erythrocytes in hydrogen peroxide

Effect of hemopoietic and other agents on the hydroxyphenyluria of premature infants

FEASIBILITY OF FRAGILE X CHROMOSOME PRENATAL DIAGNOSIS DEMONSTRATED

Split hand and foot deformity and the syndrome of ectrodactyly, ectodermal dysplasia, and clefting (EEC): A report of five patients

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