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No Evidence of False Reassurance among Women with an Inconclusive BRCA1/2 Genetic Test Result

Cancer epidemiology, biomarkers & prevention, 2005-12, Vol.14 (12), p.2862-2867

2005

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Polymorphisms in multiple genes are associated with resting heart rate in a stepwise allele-dependent manner

Heart rhythm, 2008-05, Vol.5 (5), p.694-700

2008

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Effect of heterozygosity for the methionine synthase 2756 A→G mutation on the risk for recurrent cardiovascular events

The American journal of cardiology, 2000-11, Vol.86 (10), p.1144-1146

2000

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The T-786→C Mutation in Endothelial Nitric Oxide Synthase Is Associated With Hypertension

Hypertension (Dallas, Tex. 1979), 2002-04, Vol.39 (4), p.919-922

2002

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Identification of Archaeological Animal Bone by PCR/DNA Analysis

Journal of archaeological science, 2002-01, Vol.29 (1), p.77-84

2002

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The effect of iron status on vascular health

Vascular medicine (London, England), 2006-05, Vol.11 (2), p.85-91

2006

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An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier

American journal of medical genetics. Part A, 2008-04, Vol.146A (8), p.1067-1071

2008

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Vitamin B12 decreases, but does not normalize, homocysteine and methylmalonic acid in end-stage renal disease: A link with glycine metabolism and possible explanation of hyperhomocysteinemia in end-stage renal disease

Metabolism, clinical and experimental, 2003-02, Vol.52 (2), p.168-172

2003

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Evaluation of the Quantase™ neonatal immunoreactive trypsinogen (IRT) screening assay for cystic fibrosis

Clinical chemistry and laboratory medicine, 2005-01, Vol.43 (5), p.570-572

2005

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Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH)

Pediatric research, 2000, Vol.48 (2), p.227-232

2000

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Genetic technologies, health care policy and the patent bargain

Clinical genetics, 2003-01, Vol.63 (1), p.15-18

2003

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Risk Assessment

Genetic Testing, 2005, p.340-354

2005

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Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene

American journal of human genetics, 1990-08, Vol.47 (2), p.202-217

1990

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Immunological and DNA Analysis of Blood Residues from a Surgeon's Kit used in the American Civil War

Journal of archaeological science, 1998-06, Vol.25 (6), p.553-557

1998

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The cytochrome oxidase inhibitor azide also inhibits the alternative pathway of Neurospora crassa

Canadian journal of biochemistry and cell biology, 1984-01, Vol.62 (2-3), p.129-136

1984

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Fibroblast Growth Factor Receptor-Related Skeletal Disorders

Molecular Pathology in Clinical Practice, p.109-116

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An A to T transversion at position −5 of the Factor IX promoter results in hemophilia B

Genomics (San Diego, Calif.), 1992, Vol.12 (1), p.161-163

1992

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Cosegregation of von Willebrand Factor Gene Polymorphisms and Possible Germinal Mosaicism in Type IIB von Willebrand Disease

Blood, 1991-04, Vol.77 (7), p.1476-1483

1991

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Correction of the published sequence for the human proteolipid protein gene

Human genetics, 1991-04, Vol.86 (6), p.617-618

1991

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THE MUTUAL INFLUENCE OF SPIRITUAL AND PSYCHOSOCIAL GROWTH IN THE DEVELOPMENT OF A ROMAN CATHOLIC'S SENSE OF RELIGIOUS VOCATION (PSYCHOTHERAPY, SPIRITUAL, FORMATION)

BRIDGE, PETER J

1984

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Large kindred with Ehlers-Danlos syndrome type IV due to a point mutation (G571S) in the COL3A1 gene of type III procollagen: Low risk of pregnancy complications and unexpected longevity in some affected relatives

American journal of medical genetics, 1999-02, Vol.82 (4), p.305-311

1999

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MULTIPLE Xba I POLYMORPHISMS IN HAEMOPHILIA A

British journal of haematology, 1990-06, Vol.75 (2), p.292-295

1990

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Large kindred with Ehlers-Danlos syndrome type IV due to a point mutation (G571S) in theCOL3A1 gene of type III procollagen: Low risk of pregnancy complications and unexpected longevity in some affected relatives

American journal of medical genetics, 1999-02, Vol.82 (4), p.305-311

1999

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Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA

American journal of medical genetics, 1991-03, Vol.38 (4), p.616-621

1991

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Molecular diagnosis of the fragile X [Fra (X)] syndrome: Calculation of risks based on flanking DNA markers in small phase-unknown families

American journal of medical genetics, 1989-05, Vol.33 (1), p.92-99

1989

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No Evidence of False Reassurance among Women with an Inconclusive BRCA1/2 Genetic Test Result

Polymorphisms in multiple genes are associated with resting heart rate in a stepwise allele-dependent manner

Effect of heterozygosity for the methionine synthase 2756 A→G mutation on the risk for recurrent cardiovascular events

The T-786→C Mutation in Endothelial Nitric Oxide Synthase Is Associated With Hypertension

Identification of Archaeological Animal Bone by PCR/DNA Analysis

The effect of iron status on vascular health

An undiagnosed cytogenetic abnormality results in the misidentification of a Duchenne muscular dystrophy carrier

Vitamin B12 decreases, but does not normalize, homocysteine and methylmalonic acid in end-stage renal disease: A link with glycine metabolism and possible explanation of hyperhomocysteinemia in end-stage renal disease

Evaluation of the Quantase™ neonatal immunoreactive trypsinogen (IRT) screening assay for cystic fibrosis

Further evidence for genetic heterogeneity in familial hemophagocytic lymphohistiocytosis (FHLH)

Genetic technologies, health care policy and the patent bargain

Risk Assessment

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene

Immunological and DNA Analysis of Blood Residues from a Surgeon's Kit used in the American Civil War

The cytochrome oxidase inhibitor azide also inhibits the alternative pathway of Neurospora crassa

Fibroblast Growth Factor Receptor-Related Skeletal Disorders

An A to T transversion at position −5 of the Factor IX promoter results in hemophilia B

Cosegregation of von Willebrand Factor Gene Polymorphisms and Possible Germinal Mosaicism in Type IIB von Willebrand Disease

Correction of the published sequence for the human proteolipid protein gene

THE MUTUAL INFLUENCE OF SPIRITUAL AND PSYCHOSOCIAL GROWTH IN THE DEVELOPMENT OF A ROMAN CATHOLIC'S SENSE OF RELIGIOUS VOCATION (PSYCHOTHERAPY, SPIRITUAL, FORMATION)

Large kindred with Ehlers-Danlos syndrome type IV due to a point mutation (G571S) in the COL3A1 gene of type III procollagen: Low risk of pregnancy complications and unexpected longevity in some affected relatives

MULTIPLE Xba I POLYMORPHISMS IN HAEMOPHILIA A

Large kindred with Ehlers-Danlos syndrome type IV due to a point mutation (G571S) in theCOL3A1 gene of type III procollagen: Low risk of pregnancy complications and unexpected longevity in some affected relatives

Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA

Molecular diagnosis of the fragile X [Fra (X)] syndrome: Calculation of risks based on flanking DNA markers in small phase-unknown families

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