10327244

Source:http://linkedlifedata.com/resource/pubmed/id/10327244

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008519, umls-concept:C0018220, umls-concept:C0039082, umls-concept:C0349588, umls-concept:C0524465, umls-concept:C2348519
pubmed:issue	1
pubmed:dateCreated	1999-6-28
pubmed:abstractText	We report on a male infant with distinctive facial features, short stature and rhizomelic upper limb shortening. His MRI brain scan showed abnormal ventricular architecture and bilateral periventricular nodular grey matter heterotopia (BPNH). This child represents an apparently new dysmorphic syndrome.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9207893
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0962-8827
pubmed:author	pubmed-author:ChongW KWK, pubmed-author:SlaneyS FSF, pubmed-author:WinterR MRM
pubmed:issnType	Print
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5-9
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:10327244-Body Height, pubmed-meshheading:10327244-Cerebral Ventricles, pubmed-meshheading:10327244-Facies, pubmed-meshheading:10327244-Humans, pubmed-meshheading:10327244-Infant, Newborn, pubmed-meshheading:10327244-Magnetic Resonance Imaging, pubmed-meshheading:10327244-Male, pubmed-meshheading:10327244-Syndrome
pubmed:year	1999
pubmed:articleTitle	A new syndrome of short stature, distinctive facial features and periventricular grey matter heterotopia.
pubmed:affiliation	Department of Clinical Genetics, Institute of Child Health, London, UK.
pubmed:publicationType	Journal Article, Case Reports