Source:http://linkedlifedata.com/resource/pubmed/id/17022067
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
10
|
| pubmed:dateCreated |
2006-10-24
|
| pubmed:abstractText |
Wolf-Hirschhorn syndrome (WHS), caused by the deletion of a segment in chromosome 4, is characterized by mental and developmental defects. Clinical manifestations of WHS include intrauterine growth restriction, failure to thrive in the neonatal period that is present simultaneously with hypotonia, typical "Greek helmet" facial appearance, cleft lip and palate, mental deficiency, and seizures.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Oct
|
| pubmed:issn |
1542-0752
|
| pubmed:author | |
| pubmed:copyrightInfo |
(c) 2006 Wiley-Liss, Inc.
|
| pubmed:issnType |
Print
|
| pubmed:volume |
76
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
739-43
|
| pubmed:meshHeading |
pubmed-meshheading:17022067-Abnormalities, Multiple,
pubmed-meshheading:17022067-Chromosome Deletion,
pubmed-meshheading:17022067-Chromosomes, Human, Pair 4,
pubmed-meshheading:17022067-Female,
pubmed-meshheading:17022067-Humans,
pubmed-meshheading:17022067-Nucleic Acid Hybridization,
pubmed-meshheading:17022067-Oligonucleotide Array Sequence Analysis,
pubmed-meshheading:17022067-Phenotype,
pubmed-meshheading:17022067-Pregnancy,
pubmed-meshheading:17022067-Syndrome
|
| pubmed:year |
2006
|
| pubmed:articleTitle |
Microarray-based comparative genomic hybridization analysis of Wolf-Hirschhorn syndrome in a fetus with deletion of 4p15.3 to 4pter.
|
| pubmed:affiliation |
Department of Obstetrics and Gynecology, Chang-Gung Memorial Hospital, Chang Gung University, Kwei-Shan, Tao-Yuan, Taiwan.
|
| pubmed:publicationType |
Journal Article,
Comparative Study,
Case Reports,
Research Support, Non-U.S. Gov't
|