434891

Source:http://linkedlifedata.com/resource/pubmed/id/434891

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0241888, umls-concept:C0795690, umls-concept:C0815328, umls-concept:C2745955
pubmed:issue	2
pubmed:dateCreated	1979-6-11
pubmed:abstractText	A family is described in which 4 males in two generations had omphalocele. There was no case of omphalocele in any of the women. It is suggested that the mode of inheritance could be a sex-linked recessive trait.
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/434891-13065264, http://linkedlifedata.com/resource/pubmed/commentcorrection/434891-131012, http://linkedlifedata.com/resource/pubmed/commentcorrection/434891-4442871, http://linkedlifedata.com/resource/pubmed/commentcorrection/434891-4865835
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372434
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1468-2044
pubmed:author	pubmed-author:HavaladSS, pubmed-author:NoblettHH, pubmed-author:SpeidelB DBD
pubmed:issnType	Electronic
pubmed:volume	54
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	142-3
pubmed:dateRevised	2009-11-18
pubmed:meshHeading	pubmed-meshheading:434891-Adolescent, pubmed-meshheading:434891-Female, pubmed-meshheading:434891-Hernia, Umbilical, pubmed-meshheading:434891-Humans, pubmed-meshheading:434891-Infant, Newborn, pubmed-meshheading:434891-Male, pubmed-meshheading:434891-Pedigree, pubmed-meshheading:434891-Sex Chromosome Aberrations
pubmed:year	1979
pubmed:articleTitle	Familial occurrence of omphalocele suggesting sex-linked inheritance.
pubmed:publicationType	Journal Article, Case Reports