Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22: A novel locus for a musculoskeletal syndrome

Human Genetics

Volumn 118, Issue 3-4, 2005, Pages 508-514

  Watts, Giles D J ^a   Mehta, Sarju G ^a   Zhao, Chengfeng ^b   Ramdeen, Sheena ^a   Hamilton, Sara Jane ^c   Novack, Deborah V ^d   Mumm, Steven ^d   Whyte, Michael P ^d   Mc Gillivray, Barbara ^c   Kimonis, Virginia E ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b Molecular Genetics Laboratory   (United States)

^c CHILDREN S AND WOMEN S HEALTH CENTRE OF BRITISH COLUMBIA   (Canada)

^d WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; BLOOD CLOTTING DISORDER; BONE FRAGILITY; CHROMOSOME 9P; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE COURSE; FAMILY; FEMALE; FRACTURE; FRACTURE NONUNION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; GENETIC MARKER; HAPLOTYPE; HERNIA; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; LONG BONE; MALE; MALIGNANT FIBROUS HISTIOCYTOMA; MUSCLE WEAKNESS; PRIORITY JOURNAL; SCORING SYSTEM;

EID: 30744452727     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-005-0075-z     Document Type: Article

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