8608575

Source:http://linkedlifedata.com/resource/pubmed/id/8608575

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010278, umls-concept:C0443147
pubmed:issue	11
pubmed:dateCreated	1996-5-30
pubmed:abstractText	Isolated holocalvarial synostosis with normal intelligence is described in two pairs of sibs from one kindred. Diagnosis was delayed until the age of 5 years in the pro-band. The gene carriers were asymptomatic and had no head deformity. The genetic pattern is consistent with autosomal dominant inheritance.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8503227
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0256-7040
pubmed:author	pubmed-author:Gershoni-BaruchRR, pubmed-author:PillatAA, pubmed-author:ZaaroorMM
pubmed:issnType	Print
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	617-20
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:8608575-Age of Onset, pubmed-meshheading:8608575-Child, pubmed-meshheading:8608575-Craniosynostoses, pubmed-meshheading:8608575-Female, pubmed-meshheading:8608575-Genes, Dominant, pubmed-meshheading:8608575-Humans, pubmed-meshheading:8608575-Intelligence, pubmed-meshheading:8608575-Male, pubmed-meshheading:8608575-Pedigree
pubmed:year	1995
pubmed:articleTitle	Autosomal dominant holocalvarial craniosynostosis.
pubmed:affiliation	Department of Human Genetics, Rambam Medical Center, Haifa, Israel.
pubmed:publicationType	Journal Article, Case Reports