11791880

Source:http://linkedlifedata.com/resource/pubmed/id/11791880

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0005283, umls-concept:C0009221, umls-concept:C0018591, umls-concept:C0019904, umls-concept:C0031437, umls-concept:C0079380, umls-concept:C0205082, umls-concept:C1280500
pubmed:issue	4
pubmed:dateCreated	2002-1-15
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7705865
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0363-0269
pubmed:author	pubmed-author:AltayCC, pubmed-author:BirbenEE, pubmed-author:GümrükFF, pubmed-author:GürgeyAA, pubmed-author:MergenHH, pubmed-author:OnerCC, pubmed-author:OnesSS, pubmed-author:YesilipekAA
pubmed:issnType	Print
pubmed:volume	25
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	441-5
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:11791880-Adult, pubmed-meshheading:11791880-Child, pubmed-meshheading:11791880-DNA Mutational Analysis, pubmed-meshheading:11791880-Family Health, pubmed-meshheading:11791880-Frameshift Mutation, pubmed-meshheading:11791880-Haplotypes, pubmed-meshheading:11791880-Heterozygote, pubmed-meshheading:11791880-Homozygote, pubmed-meshheading:11791880-Humans, pubmed-meshheading:11791880-Infant, pubmed-meshheading:11791880-Male, pubmed-meshheading:11791880-Phenotype, pubmed-meshheading:11791880-Promoter Regions, Genetic, pubmed-meshheading:11791880-Turkey, pubmed-meshheading:11791880-beta-Thalassemia
pubmed:year	2001
pubmed:articleTitle	Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype.
pubmed:affiliation	Department of Molecular Biology, Faculty of Science, Hacettepe University, Ankara, Turkey.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't