890090

Source:http://linkedlifedata.com/resource/pubmed/id/890090

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039082, umls-concept:C0181586, umls-concept:C0332597
pubmed:issue	3B
pubmed:dateCreated	1977-10-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0003403
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	0547-6844
pubmed:author	pubmed-author:FranckeUU, pubmed-author:MannJJ, pubmed-author:MattsonP DPD, pubmed-author:SparkesR SRS, pubmed-author:WeberFF
pubmed:issnType	Print
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	167-86
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:890090-Abnormalities, Multiple, pubmed-meshheading:890090-Acetabulum, pubmed-meshheading:890090-Child, pubmed-meshheading:890090-Child, Preschool, pubmed-meshheading:890090-Chromosome Aberrations, pubmed-meshheading:890090-Chromosome Disorders, pubmed-meshheading:890090-Chromosomes, Human, 6-12 and X, pubmed-meshheading:890090-Clavicle, pubmed-meshheading:890090-Female, pubmed-meshheading:890090-Growth Disorders, pubmed-meshheading:890090-Heart Defects, Congenital, pubmed-meshheading:890090-Humans, pubmed-meshheading:890090-Hypertelorism, pubmed-meshheading:890090-Infant, pubmed-meshheading:890090-Infant, Newborn, pubmed-meshheading:890090-Intellectual Disability, pubmed-meshheading:890090-Karyotyping, pubmed-meshheading:890090-Lip, pubmed-meshheading:890090-Male, pubmed-meshheading:890090-Pedigree, pubmed-meshheading:890090-Penis, pubmed-meshheading:890090-Pierre Robin Syndrome, pubmed-meshheading:890090-Prognosis, pubmed-meshheading:890090-Syndrome, pubmed-meshheading:890090-Translocation, Genetic
pubmed:year	1977
pubmed:articleTitle	Duplication 11 (q21 to 23 leads to qter) syndrome.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports