5504069

Source:http://linkedlifedata.com/resource/pubmed/id/5504069

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001675, umls-concept:C0010314, umls-concept:C0030705, umls-concept:C0037088, umls-concept:C0205653, umls-concept:C0426857, umls-concept:C0449721, umls-concept:C0728938, umls-concept:C1442161
pubmed:issue	5
pubmed:dateCreated	1971-4-29
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0375410
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0022-3476
pubmed:author	pubmed-author:AllderdiceP WPW, pubmed-author:BregW RWR, pubmed-author:DeCapoaAA, pubmed-author:MillerO JOJ, pubmed-author:SteeleM WMW, pubmed-author:WarburtonDD
pubmed:issnType	Print
pubmed:volume	77
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	782-91
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:5504069-Abnormalities, Multiple, pubmed-meshheading:5504069-Adolescent, pubmed-meshheading:5504069-Adult, pubmed-meshheading:5504069-Child, pubmed-meshheading:5504069-Chromosomes, Human, 4-5, pubmed-meshheading:5504069-Craniofacial Dysostosis, pubmed-meshheading:5504069-Cri-du-Chat Syndrome, pubmed-meshheading:5504069-DNA Replication, pubmed-meshheading:5504069-Female, pubmed-meshheading:5504069-Heterozygote, pubmed-meshheading:5504069-Humans, pubmed-meshheading:5504069-Karyotyping, pubmed-meshheading:5504069-Male, pubmed-meshheading:5504069-Malocclusion, pubmed-meshheading:5504069-Microcephaly, pubmed-meshheading:5504069-Middle Aged, pubmed-meshheading:5504069-Scoliosis, pubmed-meshheading:5504069-Strabismus
pubmed:year	1970
pubmed:articleTitle	The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-).
pubmed:publicationType	Journal Article