4577464

Source:http://linkedlifedata.com/resource/pubmed/id/4577464

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0086418, umls-concept:C0205549, umls-concept:C0678226, umls-concept:C1880371
pubmed:issue	4
pubmed:dateCreated	1973-9-12
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370475
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0002-9297
pubmed:author	pubmed-author:McKusickV AVA
pubmed:issnType	Print
pubmed:volume	25
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	446-56
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:4577464-Alleles, pubmed-meshheading:4577464-Genetic Complementation Test, pubmed-meshheading:4577464-Genetic Diseases, Inborn, pubmed-meshheading:4577464-Genetic Linkage, pubmed-meshheading:4577464-Humans, pubmed-meshheading:4577464-Metabolism, Inborn Errors, pubmed-meshheading:4577464-Phenotype, pubmed-meshheading:4577464-Sex Chromosomes
pubmed:year	1973
pubmed:articleTitle	Phenotypic diversity of human diseases resulting from allelic series.
pubmed:publicationType	Journal Article