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A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes

American journal of human genetics, 2007-02, Vol.80 (2), p.273-290

2007

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Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4) : Clinical description and genetic localization to chromosome 16q22.1

American journal of human genetics, 1996-08, Vol.59 (2), p.392-399

1996

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Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

American journal of human genetics, 1998-02, Vol.62 (2), p.325-333

1998

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Genome Scan for Tourette Disorder in Affected-Sibling-Pair and Multigenerational Families

American journal of human genetics, 2007-02, Vol.80 (2), p.265-272

Anon

2007

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Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia : evidence for locus heterogeneity

American journal of human genetics, 1993-07, Vol.53 (1), p.193-200

1993

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Genetic Linkage of Paget Disease of the Bone to Chromosome 18q

American journal of human genetics, 1997-11, Vol.61 (5), p.1117-1122

1997

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Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q

American journal of human genetics, 1999-02, Vol.64 (2), p.563-569

1999

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Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q

American journal of human genetics, 1996-07, Vol.59 (1), p.140-145

1996

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Autosomal dominant familial spastic paraplegia : tight linkage to chromosome 15q

American journal of human genetics, 1995, Vol.56 (1), p.188-192

1995

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Quantitative-Trait Loci on Chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 Control Variation in Levels of T and B Lymphocyte Subpopulations

American journal of human genetics, 2002-05, Vol.70 (5), p.1172-1182

2002

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Hyperparathyroidism–Jaw Tumor Syndrome: The HRPT2 Locus Is within a 0.7-cM Region on Chromosome 1q

American journal of human genetics, 1999-02, Vol.64 (2), p.518-525

1999

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Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus

American journal of human genetics, 1992-07, Vol.51 (1), p.92-100

1992

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A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12

American journal of human genetics, 1995-02, Vol.56 (2), p.408-415

1995

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A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p

American journal of human genetics, 1995-12, Vol.57 (6), p.1351-1363

1995

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Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene

American journal of human genetics, 1988, Vol.42 (1), p.38-44

1988

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Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers

American journal of human genetics, 1990-05, Vol.46 (5), p.943-949

1990

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A Large-Scale Genetic Association Study Confirms IL12B and Leads to the Identification of IL23R as Psoriasis-Risk Genes

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4) : Clinical description and genetic localization to chromosome 16q22.1

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

Genome Scan for Tourette Disorder in Affected-Sibling-Pair and Multigenerational Families

Genetic linkage analysis in familial benign (hypocalciuric) hypercalcemia : evidence for locus heterogeneity

Genetic Linkage of Paget Disease of the Bone to Chromosome 18q

Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8q

Paroxysmal dystonic choreoathetosis: tight linkage to chromosome 2q

Autosomal dominant familial spastic paraplegia : tight linkage to chromosome 15q

Quantitative-Trait Loci on Chromosomes 1, 2, 3, 4, 8, 9, 11, 12, and 18 Control Variation in Levels of T and B Lymphocyte Subpopulations

Hyperparathyroidism–Jaw Tumor Syndrome: The HRPT2 Locus Is within a 0.7-cM Region on Chromosome 1q

Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus

A gene for familial total anomalous pulmonary venous return maps to chromosome 4p13-q12

A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p

Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene

Diagnosis of neurofibromatosis I by using tightly linked, flanking DNA markers

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