11186259

Source:http://linkedlifedata.com/resource/pubmed/id/11186259

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021289, umls-concept:C0033382, umls-concept:C0205419, umls-concept:C0332285
pubmed:issue	4
pubmed:dateCreated	2001-1-17
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7705865
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Hemoglobins, Abnormal
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0363-0269
pubmed:author	pubmed-author:CottonFF, pubmed-author:GalactérosFF, pubmed-author:GulbisBB, pubmed-author:HansenVV, pubmed-author:HaumontDD, pubmed-author:JotzoKK, pubmed-author:LiuJJ, pubmed-author:MiyazakiAA, pubmed-author:ProméDD, pubmed-author:RiouJJ, pubmed-author:VertongenFF, pubmed-author:WajcmanHH
pubmed:issnType	Print
pubmed:volume	24
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	299-304
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:11186259-Amino Acid Sequence, pubmed-meshheading:11186259-Congo, pubmed-meshheading:11186259-Hemoglobins, Abnormal, pubmed-meshheading:11186259-Humans, pubmed-meshheading:11186259-Infant, Low Birth Weight, pubmed-meshheading:11186259-Infant, Newborn, pubmed-meshheading:11186259-Molecular Sequence Data, pubmed-meshheading:11186259-Point Mutation
pubmed:year	2000
pubmed:articleTitle	Hb Anderlecht [alpha20(B1)His-->Pro]: a silent variant found in a Congolese newborn.
pubmed:affiliation	Department of Clinical Chemistry, H pital Erasme, Université Libre de Bruxelles, Brussels, Belgium. fcotton@ulb.ac.be
pubmed:publicationType	Journal Article, Case Reports