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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1998-9-24
|
| pubmed:abstractText |
We report on a girl with duplication of 6q22.32 --> qter and microcephaly, frontal bossing, facial anomalies, and webbed neck. She has congenital heart disease, renal hypoplasia, and hearing loss along with severe developmental delay. Published reports of seven other patients are reviewed and compared. The most frequent anomalies include microcephaly, abnormal face, webbed neck, congenital heart disease, limb contractures, and developmental delay.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jun
|
| pubmed:issn |
0148-7299
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
30
|
| pubmed:volume |
78
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
123-6
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:9674901-Abnormalities, Multiple,
pubmed-meshheading:9674901-Chromosomes, Human, Pair 14,
pubmed-meshheading:9674901-Chromosomes, Human, Pair 6,
pubmed-meshheading:9674901-Female,
pubmed-meshheading:9674901-Humans,
pubmed-meshheading:9674901-Infant,
pubmed-meshheading:9674901-Phenotype,
pubmed-meshheading:9674901-Translocation, Genetic
|
| pubmed:year |
1998
|
| pubmed:articleTitle |
Duplication 6q22-->qter: definition of the phenotype.
|
| pubmed:affiliation |
Department of Maternal Fetal Medicine, United Hospital, St. Paul, Minnesota, USA.
|
| pubmed:publicationType |
Journal Article,
Case Reports
|