10968248

Source:http://linkedlifedata.com/resource/pubmed/id/10968248

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0011155, umls-concept:C0030274, umls-concept:C0432217, umls-concept:C0521425, umls-concept:C1533148
pubmed:issue	8
pubmed:dateCreated	2000-12-6
pubmed:abstractText	Clinical analysis and genetic investigations of new cases of Wolcott-Rallison syndrome are needed to evaluate the role of the gene(s) directly or indirectly implicated in pancreas development and in the aetiology of the syndrome.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7603873
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	0340-6199
pubmed:author	pubmed-author:CastelnauPP, pubmed-author:Diatloff-ZitoCC, pubmed-author:Le MerrerMM, pubmed-author:MarquisEE, pubmed-author:RobertJ JJJ, pubmed-author:TêteM JMJ
pubmed:issnType	Print
pubmed:volume	159
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	631-3
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:10968248-Abnormalities, Multiple, pubmed-meshheading:10968248-Child, pubmed-meshheading:10968248-Diabetes Mellitus, Type 1, pubmed-meshheading:10968248-Dwarfism, pubmed-meshheading:10968248-Exocrine Pancreatic Insufficiency, pubmed-meshheading:10968248-Female, pubmed-meshheading:10968248-Humans, pubmed-meshheading:10968248-Karyotyping, pubmed-meshheading:10968248-Osteochondrodysplasias, pubmed-meshheading:10968248-Syndrome
pubmed:year	2000
pubmed:articleTitle	Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't