|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
|
|
pubmed:dateCreated |
1985-10-17
|
|
pubmed:abstractText |
The association of postaxial polydactyly type A and congenital scalp defect in a 15-year-old severely mentally retarded male confirms the previously reported suggestion that the combination of both anomalies represents a new distinct entity with autosomal dominant inheritance and variable expression.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0340-6717
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
71
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
86-8
|
|
pubmed:dateRevised |
2011-11-17
|
|
pubmed:meshHeading |
pubmed-meshheading:4029956-Adolescent,
pubmed-meshheading:4029956-Fingers,
pubmed-meshheading:4029956-Genes, Dominant,
pubmed-meshheading:4029956-Humans,
pubmed-meshheading:4029956-Intellectual Disability,
pubmed-meshheading:4029956-Male,
pubmed-meshheading:4029956-Scalp,
pubmed-meshheading:4029956-Skull,
pubmed-meshheading:4029956-Syndrome,
pubmed-meshheading:4029956-Toes
|
|
pubmed:year |
1985
|
|
pubmed:articleTitle |
Scalp defect associated with postaxial polydactyly: confirmation of a distinct entity with autosomal dominant inheritance.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
