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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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Dopamine D4 Gene 7-Repeat Allele and Attention Deficit Hyperactivity Disorder

The American journal of psychiatry, 1999-05, Vol.156 (5), p.768-770

1999

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Dopamine D 4 Gene 7-Repeat Allele and Attention Deficit Hyperactivity Disorder

The American journal of psychiatry, 1999-05, Vol.156 (5), p.768-770

1999

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Genetic polymorphism of CYP2D6 and lung cancer risk

Cancer epidemiology, biomarkers & prevention, 1998-03, Vol.7 (3), p.215-219

1998

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Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis

Annals of neurology, 1998-03, Vol.43 (3), p.279-282

1998

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Homothallic mating type switching generates lethal chromosome breaks in rad52 strains of Saccharomyces cerevisiae [Yeast]

Molecular and Cellular Biology, 1981-06, Vol.1 (6), p.522-534

1981

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Novel mutations in the gene encoding ATP-binding cassette 1 in four Tangier disease kindreds

Journal of lipid research, 2000-03, Vol.41 (3), p.433-441

2000

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Extreme variability of expression in monozygotic twins with FSH muscular dystrophy

Neurology, 1993-02, Vol.43 (2), p.345-345

1993

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AbdA expression in Drosophila embryos

Genes & development, 1990-09, Vol.4 (9), p.1573-1587

1990

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Marfan Syndrome is Closely Linked to a Marker on Chromosome 15q1.5→q2.1

Proceedings of the National Academy of Sciences - PNAS, 1991-05, Vol.88 (10), p.4486-4488

1991

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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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Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy

Annals of neurology, 1996-06, Vol.39 (6), p.744-748

1996

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Highly polymorphic RFLP marker D4S130 (CRI-L518) maps to distal 4q

Nucleic acids research, 1991-10, Vol.19 (20), p.5802-5802

1991

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Genetic Linkage Map of Human Chromosome 7 with 63 DNA Markers

Proceedings of the National Academy of Sciences - PNAS, 1987-11, Vol.84 (22), p.8006-8010

1987

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Single copy probe CRI-L114 (D4S110) maps to 4p16.1

Nucleic acids research, 1991-04, Vol.19 (7), p.1728-1728

1991

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Cosmid probe CRI-C47 (D4S117) maps to 4p16.1

Nucleic acids research, 1991-04, Vol.19 (7), p.1728-1728

1991

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Domains of cis-interaction in the bithorax complex

Cold Spring Harbor Symposia on Quantitative Biology, 1985, Vol.50, p.173-180

1985

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Deletions and single base pair changes in the yeast mating type locus that prevent homothallic mating type conversions [Saccharomyces cerevisiae]

Proceedings of the National Academy of Sciences - PNAS, 1983-06, Vol.80 (11), p.3401-3405

1983

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Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype

Human molecular genetics, 1994-06, Vol.3 (6), p.923-926

1994

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Single copy probe CRI-L1065 (S6S21) maps to 6cen-6q21

Nucleic acids research, 1991-01, Vol.19 (1), p.199-199

1991

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Homothallic switching of Saccharomyces cerevisiae mating type genes by using a donor containing a large internal deletion

Molecular and Cellular Biology, 1985-08, Vol.5 (8), p.2154-2158

1985

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The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease

Chromosome research, 1994-05, Vol.2 (3), p.225-234

1994

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Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35 : combined analysis of an international consortium

American journal of human genetics, 1992-08, Vol.51 (2), p.396-403

1992

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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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Fundamental And Applied Biological Sciences. Psychology
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Genetics & Heredity
(15)
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Muscular Dystrophies - Genetics
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Polymorphism, Restriction Fragment Length
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Biochemistry & Molecular Biology
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Chromosomes, Human, Pair 4
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Diseases Of Striated Muscles. Neuromuscular Diseases
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Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

Dopamine D4 Gene 7-Repeat Allele and Attention Deficit Hyperactivity Disorder

Dopamine D 4 Gene 7-Repeat Allele and Attention Deficit Hyperactivity Disorder

Genetic polymorphism of CYP2D6 and lung cancer risk

Facioscapulohumeral dystrophy: A distinct regional myopathy with a novel molecular pathogenesis

Homothallic mating type switching generates lethal chromosome breaks in rad52 strains of Saccharomyces cerevisiae [Yeast]

Novel mutations in the gene encoding ATP-binding cassette 1 in four Tangier disease kindreds

Extreme variability of expression in monozygotic twins with FSH muscular dystrophy

AbdA expression in Drosophila embryos

Marfan Syndrome is Closely Linked to a Marker on Chromosome 15q1.5→q2.1

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)

Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy

Highly polymorphic RFLP marker D4S130 (CRI-L518) maps to distal 4q

Genetic Linkage Map of Human Chromosome 7 with 63 DNA Markers

Single copy probe CRI-L114 (D4S110) maps to 4p16.1

Cosmid probe CRI-C47 (D4S117) maps to 4p16.1

Domains of cis-interaction in the bithorax complex

A genetic linkage map of the human genome

Deletions and single base pair changes in the yeast mating type locus that prevent homothallic mating type conversions [Saccharomyces cerevisiae]

Identification of a new variant CYP2D6 allele with a single base deletion in exon 3 and its association with the poor metabolizer phenotype

Single copy probe CRI-L1065 (S6S21) maps to 6cen-6q21

Homothallic switching of Saccharomyces cerevisiae mating type genes by using a donor containing a large internal deletion

The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35 : combined analysis of an international consortium

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

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