844878

Source:http://linkedlifedata.com/resource/pubmed/id/844878

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0040715, umls-concept:C0241888, umls-concept:C0599718, umls-concept:C0599813, umls-concept:C0599893, umls-concept:C0795837, umls-concept:C1422411, umls-concept:C1522702, umls-concept:C1538631, umls-concept:C1825005
pubmed:issue	3
pubmed:dateCreated	1977-5-25
pubmed:abstractText	A girl with partial trisomy for the short arm of chromosome 10(p12leads to pter) due to mal chromosome segregation in the father 46,XY,t(7;10)(p22;p12) is described. The major abnormalities in this case are: mottled skin, mid-facial hypoplasia, low percentiles for weight, length, and head circumference, and club feet.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7613873
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	0340-6717
pubmed:author	pubmed-author:BachmanRR, pubmed-author:JohnsonGG, pubmed-author:RiddervoldPP, pubmed-author:RoedTT
pubmed:issnType	Print
pubmed:day	14
pubmed:volume	35
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	353-6
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:844878-Abnormalities, Multiple, pubmed-meshheading:844878-Chromosome Aberrations, pubmed-meshheading:844878-Chromosomes, Human, 6-12 and X, pubmed-meshheading:844878-Female, pubmed-meshheading:844878-Humans, pubmed-meshheading:844878-Infant, pubmed-meshheading:844878-Phenotype, pubmed-meshheading:844878-Translocation, Genetic, pubmed-meshheading:844878-Trisomy
pubmed:year	1977
pubmed:articleTitle	Partial trisomy 10p and familial translocation t(7;10)(p22;p12).
pubmed:publicationType	Journal Article, Case Reports