4345621

Source:http://linkedlifedata.com/resource/pubmed/id/4345621

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008059, umls-concept:C0008660, umls-concept:C0426857, umls-concept:C0449721, umls-concept:C1442161
pubmed:issue	1
pubmed:dateCreated	1973-3-5
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372606
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Quinidine
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	0009-9228
pubmed:author	pubmed-author:DerencsenyiAA, pubmed-author:DonnellG NGN, pubmed-author:HurstNN, pubmed-author:MavalwalaJJ, pubmed-author:ParkerC ECE
pubmed:issnType	Print
pubmed:volume	12
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	42-6
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:4345621-Age Determination by Skeleton, pubmed-meshheading:4345621-Child, Preschool, pubmed-meshheading:4345621-Chromosome Aberrations, pubmed-meshheading:4345621-Chromosome Disorders, pubmed-meshheading:4345621-Chromosomes, Human, 16-18, pubmed-meshheading:4345621-Craniofacial Dysostosis, pubmed-meshheading:4345621-Dental Caries, pubmed-meshheading:4345621-Dermatoglyphics, pubmed-meshheading:4345621-Female, pubmed-meshheading:4345621-Growth Disorders, pubmed-meshheading:4345621-Humans, pubmed-meshheading:4345621-Intellectual Disability, pubmed-meshheading:4345621-Karyotyping, pubmed-meshheading:4345621-Microscopy, Fluorescence, pubmed-meshheading:4345621-Muscle Tonus, pubmed-meshheading:4345621-Quinidine, pubmed-meshheading:4345621-Sex Factors, pubmed-meshheading:4345621-Syndrome
pubmed:year	1973
pubmed:articleTitle	A short, retarded child with a deletion of the short arm of chromosome 18 (18p-).
pubmed:publicationType	Journal Article