Complex camptopolydactyly: An unusual hand malformation

American Journal of Medical Genetics

Volumn 83, Issue 3, 1999, Pages 191-192

  Phadke, Shubha R ^a   Gautam, Prachi ^a  

^a SANJAY GANDHI POSTGRADUATE INSTITUTE OF MEDICAL SCIENCES   (India)

Author keywords

Camptopolydactyly; Hand malformations; Polydactyly

Indexed keywords

ARTICLE; BONE DEVELOPMENT; BONE MALFORMATION; CAMPTODACTYLY; CASE REPORT; CHILD; FEMALE; GENE MUTATION; HAND MALFORMATION; HAND RADIOGRAPHY; HUMAN; POLYDACTYLY; PRIORITY JOURNAL;

BONE MORPHOGENETIC PROTEINS; CHILD, PRESCHOOL; FEMALE; GENES, HOMEOBOX; HAND DEFORMITIES, CONGENITAL; HUMANS; MUTATION; POLYDACTYLY;

EID: 0033583221     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990319)83:3<191::AID-AJMG9>3.0.CO;2-W     Document Type: Article

References (4)

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2. Edwards JA, Gale RP. 1972. Camptodactyly: a new autosomal dominant trait with two probable homozygotes. Am J Hum Genet 24:464-474.
3. Muragaki Y, Mundlos S, Upton J, Oslen BR. 1996. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science 272:548-551.
4. Scott MP. 1997. Hox genes: arms and the man. Nat Genet 15:117-118.