18541966

Source:http://linkedlifedata.com/resource/pubmed/id/18541966

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005744, umls-concept:C0031437, umls-concept:C0033377, umls-concept:C0221357, umls-concept:C0439660, umls-concept:C1303003, umls-concept:C1442161
pubmed:issue	3
pubmed:dateCreated	2008-6-10
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9207893
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0962-8827
pubmed:author	pubmed-author:CroftMarion SMS, pubmed-author:TurnpennyPeter DPD
pubmed:issnType	Print
pubmed:volume	17
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	189-91
pubmed:meshHeading	pubmed-meshheading:18541966-Abnormalities, Multiple, pubmed-meshheading:18541966-Adolescent, pubmed-meshheading:18541966-Blepharophimosis, pubmed-meshheading:18541966-Blepharoptosis, pubmed-meshheading:18541966-Chromosome Deletion, pubmed-meshheading:18541966-Chromosomes, Human, Pair 3, pubmed-meshheading:18541966-Eyelids, pubmed-meshheading:18541966-Female, pubmed-meshheading:18541966-Fibrous Dysplasia, Polyostotic, pubmed-meshheading:18541966-Foot Deformities, Congenital, pubmed-meshheading:18541966-Hand Deformities, Congenital, pubmed-meshheading:18541966-Humans, pubmed-meshheading:18541966-Phenotype, pubmed-meshheading:18541966-Renal Osteodystrophy
pubmed:year	2008
pubmed:articleTitle	Deletion 3q22.1-q23 with blepharophimosis, ptosis and epicanthus inversus and an Albright hereditary osteodystrophy-like brachydactyly phenotype.
pubmed:affiliation	Department of Clinical Genetics, Royal Devon & Exeter Hospital, Exeter, UK. marion.croft@rdeft.nhs.uk
pubmed:publicationType	Journal Article, Case Reports