Hereditary multiple exostoses (EXT): Mutational studies of familial EXT1 cases and EXT-associated malignancies

American Journal of Human Genetics

Volumn 60, Issue 1, 1997, Pages 80-86

  Hecht, Jacqueline T ^a   Hogue, Deborah ^a   Wang, Yang ^a   Blanton, Susan H ^b   Wagner, Michael ^c   Strong, Louise C ^d   Raskind, Wendy ^e   Hansen, Mark F ^f   Wells, Dan ^c  

^a UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

^c UNIVERSITY OF HOUSTON   (United States)

^d UNIVERSITY OF TEXAS   (United States)

^e UNIVERSITY OF WASHINGTON   (United States)

^f BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHONDROBLASTOMA; CHONDROSARCOMA; CHROMOSOME 10Q; CHROMOSOME 11P; CHROMOSOME 19Q; CHROMOSOME 8Q; CLINICAL ARTICLE; CLINICAL PROTOCOL; CONTROLLED STUDY; FEMALE; FRAMESHIFT MUTATION; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; HEREDITARY MULTIPLE EXOSTOSIS; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MALE; PEDIGREE; PRIORITY JOURNAL; SOMATIC MUTATION;

BONE NEOPLASMS; CHONDROBLASTOMA; CHONDROSARCOMA; EXOSTOSES, MULTIPLE HEREDITARY; FEMALE; GENE DELETION; GENETIC MARKERS; HETEROZYGOTE; HUMANS; MALE; MUTATION; PEDIGREE;

EID: 0031020756     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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