8336589

Source:http://linkedlifedata.com/resource/pubmed/id/8336589

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008625, umls-concept:C1855496
pubmed:issue	2
pubmed:dateCreated	1993-8-23
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0400714
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0025-729X
pubmed:author	pubmed-author:TrentR JRJ
pubmed:issnType	Print
pubmed:day	19
pubmed:volume	159
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	128-31
pubmed:dateRevised	2005-11-16
pubmed:meshHeading	pubmed-meshheading:8336589-Angelman Syndrome, pubmed-meshheading:8336589-Chromosome Aberrations, pubmed-meshheading:8336589-Chromosome Disorders, pubmed-meshheading:8336589-Cytogenetics, pubmed-meshheading:8336589-Humans, pubmed-meshheading:8336589-Prader-Willi Syndrome
pubmed:year	1993
pubmed:articleTitle	Contiguous gene syndromes and small chromosome abnormalities.
pubmed:affiliation	Department of Molecular Genetics, Royal Prince Alfred Hospital, Camperdown, NSW.
pubmed:publicationType	Journal Article, Review