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Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

Cell, 1993-01, Vol.72 (2), p.279-290

1993

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D2 dopamine receptor gene and cigarette smoking: A reward gene?

Medical hypotheses, 1994-04, Vol.42 (4), p.257-260

1994

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Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11 : linkage to convulsions and electroencephalography trait

American journal of human genetics, 1995-08, Vol.57 (2), p.368-381

1995

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D2 and D4 dopamine receptor polymorphisms and personality

American journal of medical genetics, 1998-05, Vol.81 (3), p.257-267

1998

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The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships

The Journal of biological chemistry, 1987-11, Vol.262 (33), p.16060-16071

1987

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Assignment of the Human and Mouse Prion Protein Genes to Homologous Chromosomes

Proceedings of the National Academy of Sciences - PNAS, 1986-10, Vol.83 (19), p.7358-7362

1986

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Reactivation of an Inactive Human X Chromosome: Evidence for X Inactivation by DNA Methylation

Science (American Association for the Advancement of Science), 1981-01, Vol.211 (4480), p.393-396

1981

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Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis

Annals of neurology, 1992-06, Vol.31 (6), p.663-668

1992

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Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy

Annals of neurology, 1996-02, Vol.39 (2), p.187-195

1996

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Complementary homeo protein gradients in developing limb buds

Genes & development, 1989-05, Vol.3 (5), p.641-650

1989

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A New Locus for Autosomal Dominant Cataract on Chromosome 12q13

Investigative ophthalmology & visual science, 2000-08, Vol.41 (9), p.2665-2670

2000

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Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa

American journal of human genetics, 1996-02, Vol.58 (2), p.347-355

1996

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Lafora Progressive Myoclonus Epilepsy: Narrowing the Chromosome 6q24 Locus by Recombinations and Homozygosities

American journal of human genetics, 1997-11, Vol.61 (5), p.1205-1209

1997

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Genomic organization and chromosomal localization of a novel human hepatic dihydrodiol dehydrogenase with high affinity bile acid binding

The Journal of biological chemistry, 1994-03, Vol.269 (11), p.8416-8422

1994

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Linkage of an autosomal dominant clefting syndrome (Van der Woude) to Loci on chromosome Iq

American journal of human genetics, 1990-03, Vol.46 (3), p.486-491

1990

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Cloning of the human cholesterol 7 α-hydroxylase gene ( CYP7) and localization to chromosome 8q11–q12

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.153-161

1992

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Molecular insights into Fanconi anemia

The Journal of clinical investigation, 1996-02, Vol.97 (4), p.897-898

Sparkes, R S

1996

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The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding protein gene

The Journal of biological chemistry, 1987-02, Vol.262 (6), p.2458-2467

1987

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Regional Mapping of Human Chromosome 19: Organization of Genes for Plasma Lipid Transport (APOC1, -C2, and -E and LDLR) and the Genes C3, PEPD, and GPI

Proceedings of the National Academy of Sciences - PNAS, 1986-06, Vol.83 (11), p.3929-3933

1986

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Chromosomal localization of the human vesicular amine transporter genes

Genomics (San Diego, Calif.), 1993-12, Vol.18 (3), p.720-723

1993

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D2 dopamine receptor gene and obesity

The International journal of eating disorders, 1994-04, Vol.15 (3), p.205-217

1994

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Progress in Mapping Human Epilepsy Genes

Epilepsia (Copenhagen), 1994-01, Vol.35 (s1), p.S29-S40

1994

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Regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A synthase and the chromosomal localization of the human gene

The Journal of biological chemistry, 1986-12, Vol.261 (34), p.16249-16255

1986

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Chromosomal assignment of the human gene for the cancer-associated retinopathy protein (recoverin) to chromosome 17p13.1

Journal of neuroscience research, 1995-02, Vol.40 (2), p.165-168

1995

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The apolipoprotein(a) gene resides on human chromosome 6q26-27, in close proximity to the homologous gene for plasminogen

Human genetics, 1988-08, Vol.79 (4), p.352-356

1988

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Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

D2 dopamine receptor gene and cigarette smoking: A reward gene?

Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11 : linkage to convulsions and electroencephalography trait

D2 and D4 dopamine receptor polymorphisms and personality

The human and rodent intestinal fatty acid binding protein genes. A comparative analysis of their structure, expression, and linkage relationships

Assignment of the Human and Mouse Prion Protein Genes to Homologous Chromosomes

Reactivation of an Inactive Human X Chromosome: Evidence for X Inactivation by DNA Methylation

Startle disease, or hyperekplexia: Response to clonazepam and assignment of the gene (STHE) to chromosome 5q by linkage analysis

Clinical and genetic analysis of a large pedigree with juvenile myoclonic epilepsy

Complementary homeo protein gradients in developing limb buds

A New Locus for Autosomal Dominant Cataract on Chromosome 12q13

Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa

Lafora Progressive Myoclonus Epilepsy: Narrowing the Chromosome 6q24 Locus by Recombinations and Homozygosities

Genomic organization and chromosomal localization of a novel human hepatic dihydrodiol dehydrogenase with high affinity bile acid binding

Linkage of an autosomal dominant clefting syndrome (Van der Woude) to Loci on chromosome Iq

Cloning of the human cholesterol 7 α-hydroxylase gene ( CYP7) and localization to chromosome 8q11–q12

Molecular insights into Fanconi anemia

The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding protein gene

Regional Mapping of Human Chromosome 19: Organization of Genes for Plasma Lipid Transport (APOC1, -C2, and -E and LDLR) and the Genes C3, PEPD, and GPI

Chromosomal localization of the human vesicular amine transporter genes

D2 dopamine receptor gene and obesity

Progress in Mapping Human Epilepsy Genes

Regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A synthase and the chromosomal localization of the human gene

Chromosomal assignment of the human gene for the cancer-associated retinopathy protein (recoverin) to chromosome 17p13.1

The apolipoprotein(a) gene resides on human chromosome 6q26-27, in close proximity to the homologous gene for plasminogen

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