5619991

Source:http://linkedlifedata.com/resource/pubmed/id/5619991

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0000769, umls-concept:C0030705, umls-concept:C0439064, umls-concept:C2931809
pubmed:issue	2
pubmed:dateCreated	1969-12-5
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Blood Group Antigens
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0022-2593
pubmed:author	pubmed-author:FareedNN, pubmed-author:MerrittA DAD, pubmed-author:PalmerC GCG
pubmed:issnType	Print
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	117-23
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:5619991-Abnormalities, Multiple, pubmed-meshheading:5619991-Autoradiography, pubmed-meshheading:5619991-Blood Group Antigens, pubmed-meshheading:5619991-Bone and Bones, pubmed-meshheading:5619991-Child, pubmed-meshheading:5619991-Chromosome Aberrations, pubmed-meshheading:5619991-Chromosome Disorders, pubmed-meshheading:5619991-Chromosomes, Human, 16-18, pubmed-meshheading:5619991-Dermatoglyphics, pubmed-meshheading:5619991-Humans, pubmed-meshheading:5619991-Intellectual Disability, pubmed-meshheading:5619991-Karyotyping, pubmed-meshheading:5619991-Male
pubmed:year	1967
pubmed:articleTitle	Ring chromosome 18 in a patient with multiple anomalies.
pubmed:publicationType	Journal Article