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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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Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

Nature genetics, 1993-06, Vol.4 (2), p.165-169

1993

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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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Genomics of the Bacillus cereus group of organisms

FEMS microbiology reviews, 2005-04, Vol.29 (2), p.303-329

2005

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Assignment of SOD3 to human chromosome band 4p15.3→p15.1 with somatic cell and radiation hybrid mapping, linkage mapping, and fluorescent in-situ hybridization

Cytogenetic and genome research, 2003, Vol.101 (2), p.178C-178C

2003

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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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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 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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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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A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD)

American journal of human genetics, 1993-10, Vol.53 (4), p.874-880

1993

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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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Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13. 1-q21. 1 and mouse chromosome 5

Genomics (San Diego, Calif.), 1994-04, Vol.20:3

1994

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Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.479-485

1993

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Radiation hybrid map spanning the huntington disease gene region of chromosome 4

Genomics (San Diego, Calif.), 1992-08, Vol.13 (4), p.1040-1046

1992

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A highly polymorphic VNTR locus on the long arm of chromosome 4

Nucleic acids research, 1991-03, Vol.19 (5), p.1168-1168

1991

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The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library

Human molecular genetics, 1993-03, Vol.2 (3), p.305-309

1993

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YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene

Genomics (San Diego, Calif.), 1994-02, Vol.19 (3), p.532-541

1994

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FISH detection of Wolf-Hirschhorn syndrome : exclusion of D4F26 as critical site

American journal of medical genetics, 1994-08, Vol.52 (1), p.70-74

1994

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

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

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

Genomics of the Bacillus cereus group of organisms

Assignment of SOD3 to human chromosome band 4p15.3→p15.1 with somatic cell and radiation hybrid mapping, linkage mapping, and fluorescent in-situ hybridization

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

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

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

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

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD)

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

Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13. 1-q21. 1 and mouse chromosome 5

Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus

Radiation hybrid map spanning the huntington disease gene region of chromosome 4

A highly polymorphic VNTR locus on the long arm of chromosome 4

The isolation of cDNAs within the Huntington disease region by hybridisation of yeast artificial chromosomes to a cDNA library

YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene

FISH detection of Wolf-Hirschhorn syndrome : exclusion of D4F26 as critical site

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