9885740

Source:http://linkedlifedata.com/resource/pubmed/id/9885740

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021051, umls-concept:C0039082, umls-concept:C0040034
pubmed:issue	12
pubmed:dateCreated	1999-2-5
pubmed:abstractText	Clinical features of Jacobsen syndrome include facial dysmorphism, congenital heart defects, digit anomalies and mild to moderate psychomotor retardation. Thrombocytopenia or pancytopenia is observed in one half of patients.
pubmed:language	fre
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9421356
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0929-693X
pubmed:author	pubmed-author:FrayeMM, pubmed-author:MarianiRR, pubmed-author:MonpouxFF, pubmed-author:PedeutourFF, pubmed-author:PhilipPP, pubmed-author:SirventNN, pubmed-author:TicchioniMM, pubmed-author:Turc-CarelCC
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1338-40
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:9885740-Child, pubmed-meshheading:9885740-Chromosome Deletion, pubmed-meshheading:9885740-Chromosomes, Human, Pair 11, pubmed-meshheading:9885740-Dysgammaglobulinemia, pubmed-meshheading:9885740-Face, pubmed-meshheading:9885740-Female, pubmed-meshheading:9885740-Fingers, pubmed-meshheading:9885740-Heart Defects, Congenital, pubmed-meshheading:9885740-Humans, pubmed-meshheading:9885740-IgA Deficiency, pubmed-meshheading:9885740-Immunoglobulin M, pubmed-meshheading:9885740-Infant, pubmed-meshheading:9885740-Male, pubmed-meshheading:9885740-Psychomotor Disorders, pubmed-meshheading:9885740-Syndrome, pubmed-meshheading:9885740-Thrombocytopenia
pubmed:year	1998
pubmed:articleTitle	[Jacobsen's syndrome, thrombopenia and humoral immunodeficiency].
pubmed:affiliation	Service de pédiatrie, hôpital de l'Archet, Nice, France.
pubmed:publicationType	Journal Article, English Abstract, Case Reports