1758141

Source:http://linkedlifedata.com/resource/pubmed/id/1758141

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0332307, umls-concept:C1510455
pubmed:issue	11
pubmed:dateCreated	1992-2-6
pubmed:language	ger
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0376356
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	0023-1495
pubmed:author	pubmed-author:HinkelG KGK, pubmed-author:LorenzPP, pubmed-author:RupprechtEE, pubmed-author:TintschertSS
pubmed:issnType	Print
pubmed:volume	59
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	349-50
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:1758141-Abnormalities, Multiple, pubmed-meshheading:1758141-Acrocephalosyndactylia, pubmed-meshheading:1758141-Facial Bones, pubmed-meshheading:1758141-Humans, pubmed-meshheading:1758141-Infant, pubmed-meshheading:1758141-Syndrome
pubmed:year	1991
pubmed:articleTitle	[Pfeifer type acrocephalosyndactylia (McK 10160, 18075)].
pubmed:affiliation	Institut für Klinische Genetik, Medizinischen Akademie Carl Gustav Carus, Dresden.
pubmed:publicationType	Journal Article