|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
2
|
|
pubmed:dateCreated |
1987-11-17
|
|
pubmed:abstractText |
Three members of a nuclear family were affected by split hands and feet or syndactyly, obstructive urinary anomalies and spina bifida or diaphragmatic defect.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Oct
|
|
pubmed:issn |
0340-6717
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
77
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
203-4
|
|
pubmed:dateRevised |
2004-11-17
|
|
pubmed:meshHeading |
pubmed-meshheading:3308683-Abnormalities, Multiple,
pubmed-meshheading:3308683-Adult,
pubmed-meshheading:3308683-Diaphragm,
pubmed-meshheading:3308683-Female,
pubmed-meshheading:3308683-Genes, Dominant,
pubmed-meshheading:3308683-Hand Deformities, Congenital,
pubmed-meshheading:3308683-Humans,
pubmed-meshheading:3308683-Infant, Newborn,
pubmed-meshheading:3308683-Male,
pubmed-meshheading:3308683-Pedigree,
pubmed-meshheading:3308683-Pregnancy,
pubmed-meshheading:3308683-Spina Bifida Occulta,
pubmed-meshheading:3308683-Syndrome,
pubmed-meshheading:3308683-Ureter
|
|
pubmed:year |
1987
|
|
pubmed:articleTitle |
Split hand, obstructive urinary anomalies and spina bifida or diaphragmatic defect syndrome with autosomal dominant inheritance.
|
|
pubmed:affiliation |
Department of Human Genetics and Teratology, WHO Collaborating Centre for the Community Control of Hereditary Diseases, Budapest, Hungary.
|
|
pubmed:publicationType |
Journal Article,
Case Reports
|
