7677158

Source:http://linkedlifedata.com/resource/pubmed/id/7677158

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008445, umls-concept:C0020757, umls-concept:C0039082, umls-concept:C0086543, umls-concept:C0086582, umls-concept:C1847879
pubmed:issue	3
pubmed:dateCreated	1995-10-19
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/7677158-7677157
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7708900
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0148-7299
pubmed:author	pubmed-author:HappleRR
pubmed:issnType	Print
pubmed:day	3
pubmed:volume	57
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	493
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:7677158-Adult, pubmed-meshheading:7677158-Cataract, pubmed-meshheading:7677158-Child, Preschool, pubmed-meshheading:7677158-Chondrodysplasia Punctata, pubmed-meshheading:7677158-Genes, Dominant, pubmed-meshheading:7677158-Genetic Linkage, pubmed-meshheading:7677158-Humans, pubmed-meshheading:7677158-Ichthyosis, pubmed-meshheading:7677158-Infant, Newborn, pubmed-meshheading:7677158-Male, pubmed-meshheading:7677158-Syndrome, pubmed-meshheading:7677158-X Chromosome
pubmed:year	1995
pubmed:articleTitle	X-linked dominant chondrodysplasia punctata/ichthyosis/cataract syndrome in males.
pubmed:publicationType	Letter, Comment, Case Reports