3499855

Source:http://linkedlifedata.com/resource/pubmed/id/3499855

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021270, umls-concept:C0021943, umls-concept:C1515568, umls-concept:C1517983, umls-concept:C1956097
pubmed:issue	3
pubmed:dateCreated	1987-12-7
pubmed:abstractText	An infant was found to have a de novo complex rearrangement of one chromosome 4. Her karyotype was interpreted as 46,XX,inv del(4)(pter::p16.3::q31.2----p15.2::q31.2----qter). Clinically she showed the features of the Wolf-Hirschhorn syndrome.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370562
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0003-3995
pubmed:author	pubmed-author:BilleaudCC, pubmed-author:ChoisetAA, pubmed-author:GirardSS, pubmed-author:LongoCC, pubmed-author:SandlerBB, pubmed-author:SauraRR, pubmed-author:ServilleFF
pubmed:issnType	Print
pubmed:volume	30
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	170-4
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:3499855-Chromosome Aberrations, pubmed-meshheading:3499855-Chromosome Deletion, pubmed-meshheading:3499855-Chromosome Disorders, pubmed-meshheading:3499855-Chromosome Inversion, pubmed-meshheading:3499855-Chromosomes, Human, Pair 4, pubmed-meshheading:3499855-Female, pubmed-meshheading:3499855-Humans, pubmed-meshheading:3499855-Infant, pubmed-meshheading:3499855-Karyotyping
pubmed:year	1987
pubmed:articleTitle	De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome.
pubmed:affiliation	Centre de Génétique, Hôpital Saint-Vincent de Paul, Paris.
pubmed:publicationType	Journal Article, Case Reports