5555078

Source:http://linkedlifedata.com/resource/pubmed/id/5555078

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019425, umls-concept:C0023374, umls-concept:C0221971, umls-concept:C0439831, umls-concept:C1511790, umls-concept:C1524063
pubmed:issue	983
pubmed:dateCreated	1971-6-17
pubmed:abstractText	A method is described which permits rapid phenotypic diagnosis of the Lesch-Nyhan heterozygote by direct assay of hypoxanthine guanine phosphori-bosyltransferase activity in single hair follicles obtained from the scalp.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0404511
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Transferases
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	0036-8075
pubmed:author	pubmed-author:CampbellBB, pubmed-author:GartlerS MSM, pubmed-author:GoldsteinJ LJL, pubmed-author:ScudiJ VJV
pubmed:issnType	Print
pubmed:day	7
pubmed:volume	172
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	572-4
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:5555078-Adolescent, pubmed-meshheading:5555078-Adult, pubmed-meshheading:5555078-Child, pubmed-meshheading:5555078-Clinical Enzyme Tests, pubmed-meshheading:5555078-Female, pubmed-meshheading:5555078-Hair, pubmed-meshheading:5555078-Heterozygote, pubmed-meshheading:5555078-Humans, pubmed-meshheading:5555078-Lesch-Nyhan Syndrome, pubmed-meshheading:5555078-Male, pubmed-meshheading:5555078-Middle Aged, pubmed-meshheading:5555078-Purine-Pyrimidine Metabolism, Inborn Errors, pubmed-meshheading:5555078-Scalp, pubmed-meshheading:5555078-Self Mutilation, pubmed-meshheading:5555078-Transferases
pubmed:year	1971
pubmed:articleTitle	Lesch-Nyhan syndrome: rapid detection of heterozygotes by use of hair follicles.
pubmed:publicationType	Journal Article