A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie Tooth disease

American Journal of Human Genetics

Volumn 75, Issue 1, 2004, Pages 92-96

  Shrimpton, Antony E ^a,f   Levinsohn, E Mark ^d   Yozawitz, Justin M ^a   Packard Jr , David S ^b   Cady, Robert B ^c   Middleton, Frank A ^c   Persico, Antonio M ^e   Hootnick, David R ^b,c  

^a SUNY UPSTATE MEDICAL UNIVERSITY   (United States)

^b STATE UNIVERSITY OF NEW YORK   (United States)

^c State University of New York Upstate Medical University: College of Medicine   (United States)

^d CROUSE HOSPITAL   (United States)

^e UNIVERSITY CAMPUS BIO MEDICO   (Italy)

^f NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CAUCASIAN; CHROMOSOME 2Q; CONGENITAL FLATFOOT; CONGENITAL MALFORMATION; DNA ISOLATION; FAMILIAL DISEASE; FOOT MALFORMATION; GENE MUTATION; GENE SEQUENCE; GENETIC LINKAGE; HEREDITARY MOTOR SENSORY NEUROPATHY; HETEROZYGOSITY; HOX GENE; HOXD10 GENE; HUMAN; ITALY; LINKAGE ANALYSIS; MISSENSE MUTATION; PENETRANCE; PRIORITY JOURNAL; RARE DISEASE; SEGREGATION ANALYSIS; TALUS; WHOLE GENOME LINKAGE ANALYSIS;

EID: 3042597718     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/422015     Document Type: Article

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