Evaluation of embryonic and perinatal myosin gene mutations and the etiology of congenital idiopathic clubfoot

Journal of Pediatric Orthopaedics

Volumn 30, Issue 3, 2010, Pages 231-234

  Shyy, William ^a   Wang, Kai ^b   Sheffield, Val C ^a,c   Morcuende, Jose A ^a  

^a UNIVERSITY OF IOWA   (United States)

^b UNIVERSITY OF IOWA   (United States)

^c HOWARD HUGHES MEDICAL INSTITUTE   (United States)

Author keywords

Arthrogryposis; Clubfoot; Genetics; Myosin

Indexed keywords

DNA; MESSENGER RNA; MYOSIN;

ARTHROGRYPOSIS; ARTICLE; BIRTH DEFECT; CLINICAL ARTICLE; CLUBFOOT; CONGENITAL MALFORMATION; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DNA SEQUENCE; EMBRYO; FEMALE; GENE MUTATION; HUMAN; IDIOPATHIC DISEASE; MALE; NEWBORN; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CLUBFOOT; EXONS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MUTATION; MYOSIN HEAVY CHAINS; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA;

EID: 77950982812     PISSN: 02716798     EISSN: None     Source Type: Journal    
DOI: 10.1097/BPO.0b013e3181d35e3f     Document Type: Article

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