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Extreme variability among mammalian V1R gene families

Genome research, 2010-01, Vol.20 (1), p.10-18

2010

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Large-Scale Copy Number Polymorphism in the Human Genome

Science (American Association for the Advancement of Science), 2004-07, Vol.305 (5683), p.525-528

2004

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Array comparative genomic hybridization analysis of genomic alterations in breast cancer subtypes

Cancer research (Chicago, Ill.), 2004-12, Vol.64 (23), p.8541-8549

2004

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Stimulation of p53-mediated Transcriptional Activation by the p53-binding Proteins, 53BP1 and 53BP2

The Journal of biological chemistry, 1998-10, Vol.273 (40), p.26061-26068

1998

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Comparative mapping of the region of human chromosome 7 deleted in williams syndrome

Genome research, 1999-05, Vol.9 (5), p.428-436

1999

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Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

Human genetics, 1998-11, Vol.103 (5), p.590-599

1998

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Segmental Duplications: Organization and Impact Within the Current Human Genome Project Assembly

Genome research, 2001-06, Vol.11 (6), p.1005-1017

Bailey, J. A.

2001

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Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

Human molecular genetics, 1994-08, Vol.3 (8), p.1345-1354

1994

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Cloning and Characterization of Two Toll/Interleukin-1 Receptor–Like Genes TIL3 and TIL4: Evidence for a Multi-Gene Receptor Family in Humans

Blood, 1998-06, Vol.91 (11), p.4020-4027

1998

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Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers

Human molecular genetics, 1998-02, Vol.7 (2), p.195-202

1998

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Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes

Human molecular genetics, 1998, Vol.7 (1), p.13-26

1998

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Segmental duplications: organization and impact within the current human genome project assembly

Genome research, 2001-06, Vol.11 (6), p.1005-1017

2001

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Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family

Genome research, 1997-01, Vol.7 (1), p.10-16

1997

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Large Multi-Chromosomal Duplications Encompass Many Members of the Olfactory Receptor Gene Family in the Human Genome

Human molecular genetics, 1998-12, Vol.7 (13), p.2007-2020

1998

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Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei

American journal of human genetics, 1991, Vol.48 (1), p.1-15

1991

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Cloning and Characterization of Two Toll/Interleukin-1 Receptor–Like Genes TIL3 and TIL4: Evidence for a Multi-Gene Receptor Family in Humans

Blood, 1998-06, Vol.91 (11), p.4020-4027

1998

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A Genomic Region Encompassing a Cluster of Olfactory Receptor Genes and a Myosin Light Chain Kinase (MYLK) Gene Is Duplicated on Human Chromosome Regions 3q13–q21 and 3p13

Genomics (San Diego, Calif.), 1999-02, Vol.56 (1), p.98-110

1999

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The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney

Genomics (San Diego, Calif.), 1995-01, Vol.25 (2), p.462-468

1995

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Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients

Human genetics, 1996-12, Vol.98 (6), p.710-718

1996

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Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers

Human molecular genetics, 1994-03, Vol.3 (3), p.489-501

1994

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The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2

American journal of human genetics, 1995-04, Vol.56 (4), p.926-937

1995

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Gene Structure, Sequence, and Chromosomal Localization of the Human Red Cell-Type Low-Molecular-Weight Acid Phosphotyrosyl Phosphatase Gene, ACP1

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.133-140

1995

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A Murine Ortholog of the Human Serpin SCCA2 Maps to Chromosome 1 and Inhibits Chymotrypsin-like Serine Proteinases

Genomics (San Diego, Calif.), 1998-12, Vol.54 (2), p.297-306

1998

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An 18q− Syndrome Breakpoint Resides between the Duplicated Serpins SCCA1 and SCCA2 and Arises Via a Cryptic Rearrangement With Satellite III DNA

Human molecular genetics, 1999-01, Vol.8 (1), p.87-92

1999

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Mutations in the BRCAI-Associated RING Domain (BARD1) Gene in Primary Breast, Ovarian and Uterine Cancers

Human molecular genetics, 1998-02, Vol.7 (2), p.195-202

1998

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Extreme variability among mammalian V1R gene families

Large-Scale Copy Number Polymorphism in the Human Genome

Array comparative genomic hybridization analysis of genomic alterations in breast cancer subtypes

Stimulation of p53-mediated Transcriptional Activation by the p53-binding Proteins, 53BP1 and 53BP2

Comparative mapping of the region of human chromosome 7 deleted in williams syndrome

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

Segmental Duplications: Organization and Impact Within the Current Human Genome Project Assembly

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

Cloning and Characterization of Two Toll/Interleukin-1 Receptor–Like Genes TIL3 and TIL4: Evidence for a Multi-Gene Receptor Family in Humans

Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers

Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes

Segmental duplications: organization and impact within the current human genome project assembly

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family

Large Multi-Chromosomal Duplications Encompass Many Members of the Olfactory Receptor Gene Family in the Human Genome

Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei

Cloning and Characterization of Two Toll/Interleukin-1 Receptor–Like Genes TIL3 and TIL4: Evidence for a Multi-Gene Receptor Family in Humans

A Genomic Region Encompassing a Cluster of Olfactory Receptor Genes and a Myosin Light Chain Kinase (MYLK) Gene Is Duplicated on Human Chromosome Regions 3q13–q21 and 3p13

The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney

Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients

Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers

The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2

Gene Structure, Sequence, and Chromosomal Localization of the Human Red Cell-Type Low-Molecular-Weight Acid Phosphotyrosyl Phosphatase Gene, ACP1

A Murine Ortholog of the Human Serpin SCCA2 Maps to Chromosome 1 and Inhibits Chymotrypsin-like Serine Proteinases

An 18q− Syndrome Breakpoint Resides between the Duplicated Serpins SCCA1 and SCCA2 and Arises Via a Cryptic Rearrangement With Satellite III DNA

Mutations in the BRCAI-Associated RING Domain (BARD1) Gene in Primary Breast, Ovarian and Uterine Cancers

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