21383552

Source:http://linkedlifedata.com/resource/pubmed/id/21383552

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0030705, umls-concept:C0596790, umls-concept:C1442161, umls-concept:C1855585
pubmed:issue	2
pubmed:dateCreated	2011-3-8
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9207893
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1473-5717
pubmed:author	pubmed-author:DixitAbhijitA, pubmed-author:MartinKateK, pubmed-author:SmithNigelN, pubmed-author:SuriMohnishM, pubmed-author:TantelesGeorge AGA
pubmed:issnType	Electronic
pubmed:volume	20
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	61-5
pubmed:meshHeading	pubmed-meshheading:21383552-Abnormalities, Multiple, pubmed-meshheading:21383552-Adolescent, pubmed-meshheading:21383552-Cervical Vertebrae, pubmed-meshheading:21383552-Chromosome Deletion, pubmed-meshheading:21383552-Chromosome Disorders, pubmed-meshheading:21383552-Chromosomes, Human, Pair 13, pubmed-meshheading:21383552-Comparative Genomic Hybridization, pubmed-meshheading:21383552-Craniosynostoses, pubmed-meshheading:21383552-Facial Asymmetry, pubmed-meshheading:21383552-Heart Murmurs, pubmed-meshheading:21383552-Humans, pubmed-meshheading:21383552-Hypertrichosis, pubmed-meshheading:21383552-Male, pubmed-meshheading:21383552-Phenotype, pubmed-meshheading:21383552-Torticollis
pubmed:year	2011
pubmed:articleTitle	Mild phenotype in a patient with a de-novo 2.9-Mb interstitial deletion at 13q12.11.
pubmed:affiliation	Clinical Genetics Service, City Hospital Campus, Nottingham University Hospitals, Nottingham, UK.
pubmed:publicationType	Journal Article, Case Reports