19339009

Source:http://linkedlifedata.com/resource/pubmed/id/19339009

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015295, umls-concept:C0026882, umls-concept:C0043210, umls-concept:C0085215, umls-concept:C0165602, umls-concept:C0332197, umls-concept:C0422792, umls-concept:C1414828
pubmed:issue	3
pubmed:dateCreated	2009-5-4
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0210174
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Receptors, FSH
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	1879-3479
pubmed:author	pubmed-author:KanthVishnubhotla Venkata RaviVV, pubmed-author:PrakashGolla JayaGJ, pubmed-author:RozatiRoyaR, pubmed-author:ShellingAndrew NAN, pubmed-author:SujathaMadireddiM
pubmed:issnType	Electronic
pubmed:volume	105
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	265-6
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:19339009-Adult, pubmed-meshheading:19339009-Base Sequence, pubmed-meshheading:19339009-Exons, pubmed-meshheading:19339009-Female, pubmed-meshheading:19339009-Humans, pubmed-meshheading:19339009-India, pubmed-meshheading:19339009-Mutation, pubmed-meshheading:19339009-Polymorphism, Restriction Fragment Length, pubmed-meshheading:19339009-Primary Ovarian Insufficiency, pubmed-meshheading:19339009-Receptors, FSH, pubmed-meshheading:19339009-Sequence Analysis, DNA
pubmed:year	2009
pubmed:articleTitle	Absence of 566C>T mutation in exon 7 of the FSHR gene in Indian women with premature ovarian failure.
pubmed:affiliation	Department of Clinical Genetics, Institute of Genetics and Hospital for Genetic Diseases, Osmania University, Begumpet, Hyderabad, India.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't