Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1997-3-18
|
| pubmed:abstractText |
We report on an infant girl with Hirschsprung disease, postaxial polydactyly, and atrial septal defect who was born to a consanguineous Iraqi couple. A similar condition of aganglionic megacolon, postaxial polydactyly, and ventricular septal defect with a presumed autosomal recessive (AR) inheritance was reported by Laurence in two sibs [Laurence et al.; J Med Genet 12: 334-338, 1975].
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jan
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
10
|
| pubmed:volume |
68
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
74-5
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:8986280-Abnormalities, Multiple,
pubmed-meshheading:8986280-Female,
pubmed-meshheading:8986280-Heart Septal Defects, Atrial,
pubmed-meshheading:8986280-Hirschsprung Disease,
pubmed-meshheading:8986280-Humans,
pubmed-meshheading:8986280-Infant, Newborn,
pubmed-meshheading:8986280-Polydactyly
|
| pubmed:year |
1997
|
| pubmed:articleTitle |
Hirschsprung disease, postaxial polydactyly, and atrial septal defect.
|
| pubmed:affiliation |
Division of Clinical Genetics, Hospital for Sick Children, Toronto, Ontario, Canada.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|