10210708

Source:http://linkedlifedata.com/resource/pubmed/id/10210708

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015780, umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0271623, umls-concept:C1314792, umls-concept:C1417820, umls-concept:C1845977
pubmed:issue	16
pubmed:dateCreated	1999-4-22
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0255562
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Gonadotropins
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0028-4793
pubmed:author	pubmed-author:BaronJJ, pubmed-author:CutlerG BGBJr, pubmed-author:MenkeH HHH, pubmed-author:TajimaTT
pubmed:issnType	Print
pubmed:day	22
pubmed:volume	340
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1248-52
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:10210708-Adolescent, pubmed-meshheading:10210708-Adrenal Hyperplasia, Congenital, pubmed-meshheading:10210708-Female, pubmed-meshheading:10210708-Genes, Recessive, pubmed-meshheading:10210708-Genetic Linkage, pubmed-meshheading:10210708-Gonadotropins, pubmed-meshheading:10210708-Humans, pubmed-meshheading:10210708-Hypogonadism, pubmed-meshheading:10210708-Male, pubmed-meshheading:10210708-Middle Aged, pubmed-meshheading:10210708-Pedigree, pubmed-meshheading:10210708-Phenotype, pubmed-meshheading:10210708-Point Mutation, pubmed-meshheading:10210708-Sequence Analysis, DNA, pubmed-meshheading:10210708-X Chromosome
pubmed:year	1999
pubmed:articleTitle	Hypogonadotropic hypogonadism in a female caused by an X-linked recessive mutation in the DAX1 gene.
pubmed:affiliation	Developmental Endocrinology Branch, National Institute of Child Health and Human Development, U.S. Public Health Service, Bethesda, MD 20892-1862, USA. deborah_merke@nih.gov
pubmed:publicationType	Journal Article, Case Reports