|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2006-3-6
|
|
pubmed:abstractText |
We report an atypical case of a fetus presenting with a combined achondroplasia and multiple craniosynostosis phenotype.
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|
pubmed:language |
eng
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|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0197-3851
|
|
pubmed:author |
|
|
pubmed:copyrightInfo |
2006 John Wiley & Sons, Ltd.
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
26
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
258-61
|
|
pubmed:dateRevised |
2009-11-19
|
|
pubmed:meshHeading |
pubmed-meshheading:16475234-Achondroplasia,
pubmed-meshheading:16475234-Adult,
pubmed-meshheading:16475234-Craniosynostoses,
pubmed-meshheading:16475234-Exons,
pubmed-meshheading:16475234-Female,
pubmed-meshheading:16475234-Fetal Diseases,
pubmed-meshheading:16475234-Humans,
pubmed-meshheading:16475234-Mutation,
pubmed-meshheading:16475234-Pregnancy,
pubmed-meshheading:16475234-Receptor, Fibroblast Growth Factor, Type 3,
pubmed-meshheading:16475234-Ultrasonography, Prenatal
|
|
pubmed:year |
2006
|
|
pubmed:articleTitle |
Prenatal diagnosis of achondroplasia presenting with multiple-suture synostosis: a novel association.
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|
pubmed:affiliation |
Department of Genetics and Molecular Biology, Mitera Maternity and Surgical Center, Athens, Greece.
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|
pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|
