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WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

Human molecular genetics, 1998-07, Vol.7 (7), p.1071-1082

1998

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A Transcript Map of the Newly Defined 165 kb Wolf-Hirschhorn Syndrome Critical Region

Human molecular genetics, 1997-02, Vol.6 (2), p.317-324

1997

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Reduced Penetrance of the Huntington's Disease Mutation

Human molecular genetics, 1997-05, Vol.6 (5), p.775-779

1997

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Genomic organization of the human fibroblast growth factor receptor 3 (FGFR3) gene and comparative sequence analysis with the mouse Fgfr3 gene

Genomics (San Diego, Calif.), 1997-04, Vol.41 (1), p.10-16

1997

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Comparative Analysis of a Novel Gene from the Wolf–Hirschhorn/Pitt–Rogers–Danks Syndrome Critical Region

Genomics (San Diego, Calif.), 1999-07, Vol.59 (2), p.203-212

1999

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Actinin-Associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs

The Journal of cell biology, 1997-10, Vol.139 (2), p.507-515

1997

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An integrated physical map of human chromosome 16

Nature (London), 1995-09, Vol.377 (6547 Suppl), p.335-335

1995

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Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4

American journal of human genetics, 1991-12, Vol.49 (6), p.1235-1242

1991

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The Evolutionary Distribution and Structural Organization of the Homeobox-Containing Repeat D4Z4 Indicates a Functional Role for the Ancestral Copy in the FSHD Region

Human molecular genetics, 1996-10, Vol.5 (10), p.1567-1575

1996

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A YAC Contig Spanning a Cluster of Human Type III Receptor Protein Tyrosine Kinase Genes (PDGFRA-KIT-KDR) in Chromosome Segment 4q12

Genomics (San Diego, Calif.), 1994-07, Vol.22 (2), p.431-436

1994

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Molecular Cloning, cDNA Structure, and Chromosomal Localization of the Human Type II cGMP-Dependent Protein Kinase

Biochemical and biophysical research communications, 1996-03, Vol.220 (3), p.759-765

1996

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Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel

The Journal of biological chemistry, 1992-03, Vol.267 (9), p.6257-6262

1992

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A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.1133-1142

1991

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Evaluation of the host transcriptional response to human cytomegalovirus infection

Physiological genomics, 2004-06, Vol.18 (1), p.51-62

2004

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Human chromosomal localization of genes encoding the gamma 1 and gamma 2 subunits of the gamma-aminobutyric acid receptor indicates that members of this gene family are often clustered in the genome

Proceedings of the National Academy of Sciences - PNAS, 1992-07, Vol.89 (13), p.5857-5861

1992

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Genetic mapping of the dentinogenesis imperfecta type II locus

American journal of human genetics, 1995-10, Vol.57 (4), p.832-839

1995

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Genomic Organization of the Mouse Fibroblast Growth Factor Receptor 3 (Fgfr3) Gene

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.157-162

1995

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A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat

Journal of medical genetics, 1995-01, Vol.32 (1), p.65-67

1995

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Genetic and physical maps of human chromosome 4 based on dinucleotide repeats

Genomics (San Diego, Calif.), 1992, Vol.14 (2), p.209-219

1992

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Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic cases

Neurology, 1993-11, Vol.43 (11), p.2369-2369

1993

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Genomics of the Bacillus cereus group of organisms

FEMS microbiology reviews, 2005, Vol.29 (2), p.303-329

2005

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"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype

American journal of medical genetics, 1999-02, Vol.82 (5), p.371-375

1999

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High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q

Human molecular genetics, 1994-10, Vol.3 (10), p.1801-1805

1994

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Mapping of the Gene for the Mel1a-Melatonin Receptor to Human Chromosome 4 (MTNR1A) and Mouse Chromosome 8 (Mtnr1a)

Genomics (San Diego, Calif.), 1995-05, Vol.27 (2), p.355-357

1995

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Bone morphogenetic protein: Chromosomal localization of human genes for BMP1, BMP2A, and BMP3

Genomics (San Diego, Calif.), 1991-02, Vol.9 (2), p.283-289

1991

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WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

A Transcript Map of the Newly Defined 165 kb Wolf-Hirschhorn Syndrome Critical Region

Reduced Penetrance of the Huntington's Disease Mutation

Genomic organization of the human fibroblast growth factor receptor 3 (FGFR3) gene and comparative sequence analysis with the mouse Fgfr3 gene

Comparative Analysis of a Novel Gene from the Wolf–Hirschhorn/Pitt–Rogers–Danks Syndrome Critical Region

Actinin-Associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs

An integrated physical map of human chromosome 16

Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4

The Evolutionary Distribution and Structural Organization of the Homeobox-Containing Repeat D4Z4 Indicates a Functional Role for the Ancestral Copy in the FSHD Region

A YAC Contig Spanning a Cluster of Human Type III Receptor Protein Tyrosine Kinase Genes (PDGFRA-KIT-KDR) in Chromosome Segment 4q12

Molecular Cloning, cDNA Structure, and Chromosomal Localization of the Human Type II cGMP-Dependent Protein Kinase

Primary structure and chromosomal localization of human and mouse rod photoreceptor cGMP-gated cation channel

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4

Evaluation of the host transcriptional response to human cytomegalovirus infection

Human chromosomal localization of genes encoding the gamma 1 and gamma 2 subunits of the gamma-aminobutyric acid receptor indicates that members of this gene family are often clustered in the genome

Genetic mapping of the dentinogenesis imperfecta type II locus

Genomic Organization of the Mouse Fibroblast Growth Factor Receptor 3 (Fgfr3) Gene

A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat

Genetic and physical maps of human chromosome 4 based on dinucleotide repeats

Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic cases

Genomics of the Bacillus cereus group of organisms

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q

Mapping of the Gene for the Mel1a-Melatonin Receptor to Human Chromosome 4 (MTNR1A) and Mouse Chromosome 8 (Mtnr1a)

Bone morphogenetic protein: Chromosomal localization of human genes for BMP1, BMP2A, and BMP3

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