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Asymptomatic Maternal Combined Homocystinuria and Methylmalonic Aciduria ( cblC ) Detected through Low Carnitine Levels on Newborn Screening

The Journal of pediatrics, 2009-12, Vol.155 (6), p.924-927

2009

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Pooled Analysis and Meta-analysis of Glutathione S-Transferase M1 and Bladder Cancer: A HuGE Review

American journal of epidemiology, 2002-07, Vol.156 (2), p.95-109

2002

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Prostaglandin H Synthase 2 Variant (Val511Ala) in African Americans May Reduce the Risk for Colorectal Neoplasia

Cancer epidemiology, biomarkers & prevention, 2002-11, Vol.11 (11), p.1305-1315

2002

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Costello syndrome with pancreatic islet cell hyperplasia

American journal of medical genetics, 2004-11, Vol.130A (4), p.402-405

2004

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Acetylation polymorphism and prevalence of colorectal adenomas

Cancer research (Chicago, Ill.), 1995-05, Vol.55 (10), p.2017-2020

1995

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Glutathione transferase (GSTM1) null genotype, smoking, and prevalence of colorectal adenomas

Cancer research (Chicago, Ill.), 1995-03, Vol.55 (6), p.1224-1226

1995

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Breast cancer, heterocyclic aromatic amines from meat and N-acetyltransferase 2 genotype

Carcinogenesis (New York), 2000-04, Vol.21 (4), p.607-615

2000

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Lack of association between the polyadenylation polymorphism in the NAT1 (acetyltransferase 1) gene and colorectal adenomas

Carcinogenesis (New York), 1996-10, Vol.17 (10), p.2125-2129

1996

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Hematopoietic prostaglandin D synthase suppresses intestinal adenomas in ApcΜιn/+ mice

Cancer research (Chicago, Ill.), 2007, Vol.67 (3), p.881-889

2007

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Breast cancer, passive and active cigarette smoking and N-acetyltransferase 2 genotype

Pharmacogenetics (London), 2000-07, Vol.10 (5), p.461-469

2000

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Glutathione transferase GSTT1, broccoli, and prevalence of colorectal adenomas

Pharmacogenetics (London), 2002-03, Vol.12 (2), p.175-179

2002

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PAGOD syndrome: Eighth case and comparison to animal models of congenital vitamin A deficiency

American journal of medical genetics, 2002-03, Vol.108 (3), p.229-234

2002

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Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 1992-02, Vol.85 (2), p.635-647

1992

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Genetic evidence of dissociation (generational skips) of electrical from morphologic forms of hypertrophic cardiomyopathy

The American journal of cardiology, 1990-09, Vol.66 (5), p.627-631

1990

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Variants of N-acetyltransferase NAT1 and a case-control study of colorectal adenomas

Pharmacogenetics (London), 1998-06, Vol.8 (3), p.269

1998

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Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathy

Clinical genetics, 1985-09, Vol.28 (3), p.185-198

1985

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Disease risk estimates from marker association data: Application to individuals at risk for hemochromatosis

Clinical genetics, 1985-02, Vol.27 (2), p.127-133

1985

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Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients

American journal of medical genetics, 1993-03, Vol.45 (6), p.761-763

1993

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Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals

American journal of medical genetics, 2004, Vol.130A (4), p.331-339

2004

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Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: Case report and review of triplications and their possible mechanism

American journal of medical genetics, 1999-02, Vol.82 (4), p.312-317

1999

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Anomalous inferior and superior venae cavae with oculoauriculovertebral defect: Review of Goldenhar complex and malformations of left-right asymmetry

American journal of medical genetics, 1998-01, Vol.75 (1), p.88-94

1998

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Microdontia with severe microcephaly and short stature in two brothers: Osteodysplastic primordial dwarfism with dental findings

American journal of medical genetics, 1995-08, Vol.58 (2), p.136-142

1995

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DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): A new patient and delineation of neurologic variability among recessive cases

American journal of medical genetics, 1993-09, Vol.47 (4), p.534-539

1993

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Occipital encephalocele and MURCS association: Case report and review of central nervous system anomalies in MURCS patients

American journal of medical genetics, 1996-01, Vol.61 (1), p.59-62

1996

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Omphalocele with absent radial ray (ORR): A case with diploid-triploid mixoploidy

American journal of medical genetics, 1998-01, Vol.75 (3), p.235-239

1998

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Asymptomatic Maternal Combined Homocystinuria and Methylmalonic Aciduria ( cblC ) Detected through Low Carnitine Levels on Newborn Screening

Pooled Analysis and Meta-analysis of Glutathione S-Transferase M1 and Bladder Cancer: A HuGE Review

Prostaglandin H Synthase 2 Variant (Val511Ala) in African Americans May Reduce the Risk for Colorectal Neoplasia

Costello syndrome with pancreatic islet cell hyperplasia

Acetylation polymorphism and prevalence of colorectal adenomas

Glutathione transferase (GSTM1) null genotype, smoking, and prevalence of colorectal adenomas

Breast cancer, heterocyclic aromatic amines from meat and N-acetyltransferase 2 genotype

Lack of association between the polyadenylation polymorphism in the NAT1 (acetyltransferase 1) gene and colorectal adenomas

Hematopoietic prostaglandin D synthase suppresses intestinal adenomas in ApcΜιn/+ mice

Breast cancer, passive and active cigarette smoking and N-acetyltransferase 2 genotype

Glutathione transferase GSTT1, broccoli, and prevalence of colorectal adenomas

PAGOD syndrome: Eighth case and comparison to animal models of congenital vitamin A deficiency

Evidence of genetic heterogeneity in five kindreds with familial hypertrophic cardiomyopathy

Genetic evidence of dissociation (generational skips) of electrical from morphologic forms of hypertrophic cardiomyopathy

Variants of N-acetyltransferase NAT1 and a case-control study of colorectal adenomas

Use of HLA marker associations and HLA haplotype linkage to estimate disease risks in families with gluten-sensitive enteropathy

Disease risk estimates from marker association data: Application to individuals at risk for hemochromatosis

Exstrophy of the cloaca in a 47,XXX child: Review of genitourinary malformations in triple-X patients

Chromosome 2q terminal deletion: Report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals

Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: Case report and review of triplications and their possible mechanism

Anomalous inferior and superior venae cavae with oculoauriculovertebral defect: Review of Goldenhar complex and malformations of left-right asymmetry

Microdontia with severe microcephaly and short stature in two brothers: Osteodysplastic primordial dwarfism with dental findings

DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): A new patient and delineation of neurologic variability among recessive cases

Occipital encephalocele and MURCS association: Case report and review of central nervous system anomalies in MURCS patients

Omphalocele with absent radial ray (ORR): A case with diploid-triploid mixoploidy

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