16575894

Source:http://linkedlifedata.com/resource/pubmed/id/16575894

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008928, umls-concept:C0030705, umls-concept:C0239307, umls-concept:C0444598, umls-concept:C0678257, umls-concept:C0684224, umls-concept:C0700287, umls-concept:C1257890, umls-concept:C1511726, umls-concept:C1513380
pubmed:issue	9
pubmed:dateCreated	2006-4-24
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/16575894-16222673
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Core Binding Factor Alpha 1 Subunit
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1552-4825
pubmed:author	pubmed-author:AkninJean-JacquesJJ, pubmed-author:BaumertUweU, pubmed-author:GolanIlanI, pubmed-author:MuessigDieterD, pubmed-author:RedlichMeirM
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	140
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1030
pubmed:meshHeading	pubmed-meshheading:16575894-Cleidocranial Dysplasia, pubmed-meshheading:16575894-Core Binding Factor Alpha 1 Subunit, pubmed-meshheading:16575894-European Continental Ancestry Group, pubmed-meshheading:16575894-Genotype, pubmed-meshheading:16575894-Humans, pubmed-meshheading:16575894-Mutation, pubmed-meshheading:16575894-Phenotype
pubmed:year	2006
pubmed:articleTitle	Clarification of data reported in "cleidocranial dysplasia: molecular genetic analysis and phenotypic-based description of a Middle European patient group" (AJMG 139A:78-85).
pubmed:publicationType	Letter, Comment