4235163

Source:http://linkedlifedata.com/resource/pubmed/id/4235163

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013080, umls-concept:C0040715, umls-concept:C0241888, umls-concept:C0439750, umls-concept:C0599718, umls-concept:C0599813, umls-concept:C0599893, umls-concept:C0678227, umls-concept:C1513354, umls-concept:C1522702, umls-concept:C1524003, umls-concept:C1834741
pubmed:issue	6
pubmed:dateCreated	1969-1-8
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0370471
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Blood Group Antigens
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	0002-922X
pubmed:author	pubmed-author:WeissLL, pubmed-author:WolfC BCB
pubmed:issnType	Print
pubmed:volume	116
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	609-14
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:4235163-Adult, pubmed-meshheading:4235163-Blood Group Antigens, pubmed-meshheading:4235163-Child, pubmed-meshheading:4235163-Chromosome Aberrations, pubmed-meshheading:4235163-Chromosomes, Human, 13-15, pubmed-meshheading:4235163-Chromosomes, Human, 21-22 and Y, pubmed-meshheading:4235163-Chromosomes, Human, 6-12 and X, pubmed-meshheading:4235163-Dermatoglyphics, pubmed-meshheading:4235163-Down Syndrome, pubmed-meshheading:4235163-Duodenal Obstruction, pubmed-meshheading:4235163-Female, pubmed-meshheading:4235163-Heart Defects, Congenital, pubmed-meshheading:4235163-Humans, pubmed-meshheading:4235163-Hyperbilirubinemia, pubmed-meshheading:4235163-Infant, Newborn, pubmed-meshheading:4235163-Karyotyping, pubmed-meshheading:4235163-Male, pubmed-meshheading:4235163-Mitosis, pubmed-meshheading:4235163-Mosaicism, pubmed-meshheading:4235163-Pedigree, pubmed-meshheading:4235163-Sex Chromosomes
pubmed:year	1968
pubmed:articleTitle	Familial C-G translocation causing mitotic nondisjunction. A cause of familial mosaic Down's syndrome.
pubmed:publicationType	Journal Article