reference/449890

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/449890

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	2494
issn	1552-4825 1552-4833
issueIdentifier	10
pageRange	2487-2494
publicationName	American journal of medical genetics. Part A
startingPage	2487
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bibliographicCitation	Harrison SM, Campbell IM, Keays M, Granberg CF, Villanueva C, Tannin G, Zinn AR, Castrillon DH, Shaw CA, Stankiewicz P, Baker LA. Screening and familial characterization of copy‐number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure. American J of Med Genetics Pt A. 2013 Aug 05;161(10):2487–94. doi: 10.1002/ajmg.a.36084.
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date	2013-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC3788034 https://doi.org/10.1002/ajmg.a.36084 https://pubmed.ncbi.nlm.nih.gov/23918653
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Screening and familial characterization of copy‐number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure
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Incoming Links

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Total number of triples: 68.