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Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization

Author

Cisca Wijmenga

Published in: Genomics

Date of publication: April 1, 1991

Main subject: facioscapulohumeral muscular dystrophy

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Cites articles 12

Date

Title

Authors

January 1, 1973

Release of infectious Epstein-Barr virus by transformed marmoset leukocytes
October 1, 1983

Linkage analysis and family classification under heterogeneity
July 1983

Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination
April 1984

Genomic sequencing
February 1, 1985

An algorithm to improve the computational efficiency of genetic linkage analysis
September 1, 1986

Hearing loss in facioscapulohumeral dystrophy
May 1986

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
June 1, 1987

Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications
August 1, 1989

Recombination events suggest potential sites for the Huntington's disease gene
May 1, 1989

Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139]
February 1, 1990

Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5
September 1, 1990

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

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