Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37

Human Molecular Genetics

Volumn 5, Issue 7, 1996, Pages 1043-1046

  Speer, Marcy C ^a   Tandan, Rup ^b   Rao, P Nagesh ^c   Fries, Timothy ^b   Stajich, Jeffrey M ^a   Bolhuis, Pieter A ^d   Jöbsis, G Joost ^d   Vance, Jeffery M ^a   Viles, Kristi D ^a   Sheffield, Karen ^e   James, Christi ^a   Kahler, Stephen G ^a   Pettenati, Mark ^c   Gilbert, John R ^a   Denton, Peter H ^a   Yamaoka, Larry H ^a   Pericak Vance, Margaret A ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b FLETCHER ALLEN HEALTH CARE   (United States)

^c WAKE FOREST SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF AMSTERDAM   (Netherlands)

^e SOUTHWEST FOUNDATION FOR BIOMEDICAL RESEARCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 6;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 2Q; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; JOINT CONTRACTURE; MALE; MYOPATHY; PRIORITY JOURNAL;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 2; COLLAGEN; FEMALE; GENES; GENETIC HETEROGENEITY; GENETIC MARKERS; HUMANS; LINKAGE (GENETICS); MALE; NEUROMUSCULAR DISEASES; PEDIGREE;

EID: 8944254698     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.7.1043     Document Type: Article

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