Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1982-1-9
|
pubmed:abstractText |
An Indian family was observed with postaxial polycactyly in four generations. Of the twelve affected cases, eleven were male and one was female. The affected males showed postaxial polydactyly Type A in both hands and feet. The affected female showed polysyndactyly and both Types A and B postaxial polydactyly. Study of this family strongly suggests a common causal factor for postaxial polydactyly Types A and B and polysyndactyly. The observations also support an autosomal dominant pattern of inheritance and a high degree of genetic heterogeneity in ths malformation.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0009-9163
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
20
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
36-9
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:7296946-Abnormalities, Multiple,
pubmed-meshheading:7296946-Female,
pubmed-meshheading:7296946-Fingers,
pubmed-meshheading:7296946-Genes, Dominant,
pubmed-meshheading:7296946-Humans,
pubmed-meshheading:7296946-Male,
pubmed-meshheading:7296946-Pedigree,
pubmed-meshheading:7296946-Toes
|
pubmed:year |
1981
|
pubmed:articleTitle |
An Indian family with postaxial polydactyly in four generations.
|
pubmed:publicationType |
Journal Article
|