Clinical analysis of a variant of Freeman-Sheldon syndrome (DA2B)

American Journal of Medical Genetics

Volumn 76, Issue 1, 1998, Pages 93-98

  Krakowiak, Patrycja A ^a   Bohnsack, John F ^b   Carey, John C ^b   Bamshad, Michael ^b,c  

^a UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^c SHRINERS HOSPITALS FOR CHILDREN   (United States)

Author keywords

Clubfoot; Congenital contractures; DA2B; Distal arthrogryposis; Freeman Sheldon syndrome

Indexed keywords

ARTHROGRYPOSIS; ARTICLE; BONE MALFORMATION; CHILD; CLINICAL ARTICLE; CLUBFOOT; FEMALE; FREEMAN SHELDON SYNDROME; HUMAN; JOINT CONTRACTURE; MALE; MULTIPLE MALFORMATION SYNDROME; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; ADULT; ARTHROGRYPOSIS; CHILD; CRANIOFACIAL ABNORMALITIES; FEMALE; GENES, DOMINANT; HUMANS; INFANT; MALE; PEDIGREE; PHENOTYPE; SYNDROME;

EID: 0032568081     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980226)76:1<93::AID-AJMG17>3.0.CO;2-K     Document Type: Article

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