1770527

Source:http://linkedlifedata.com/resource/pubmed/id/1770527

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002312, umls-concept:C0039082, umls-concept:C0332281, umls-concept:C1136249, umls-concept:C1704788
pubmed:issue	11
pubmed:dateCreated	1992-2-24
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-1770528, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-1770529, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-1770530, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-1941971, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-2136787, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-2225071, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-2231651, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-2339704, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-2352265, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-2649166, http://linkedlifedata.com/resource/pubmed/commentcorrection/1770527-6267462
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Globins, http://linkedlifedata.com/resource/pubmed/chemical/Hemoglobin H
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0022-2593
pubmed:author	pubmed-author:GibbonsR JRJ, pubmed-author:HiggsD RDR, pubmed-author:WeatherallD JDJ, pubmed-author:WilkieA OAO
pubmed:issnType	Print
pubmed:volume	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	729-33
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:1770527-Female, pubmed-meshheading:1770527-Genetic Linkage, pubmed-meshheading:1770527-Globins, pubmed-meshheading:1770527-Hemoglobin H, pubmed-meshheading:1770527-Heterozygote, pubmed-meshheading:1770527-Humans, pubmed-meshheading:1770527-Intellectual Disability, pubmed-meshheading:1770527-Male, pubmed-meshheading:1770527-Syndrome, pubmed-meshheading:1770527-Thalassemia, pubmed-meshheading:1770527-Transcriptional Activation, pubmed-meshheading:1770527-X Chromosome
pubmed:year	1991
pubmed:articleTitle	A newly defined X linked mental retardation syndrome associated with alpha thalassaemia.
pubmed:affiliation	MRC Molecular Haematology Unit, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford.
pubmed:publicationType	Journal Article, Review, Research Support, Non-U.S. Gov't