reference/13158957

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13158957

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	14
issn	1423-0062 0001-5652
issueIdentifier	1
pageRange	9-14
publicationName	Human Heredity
startingPage	9
bibliographicCitation	Bachega TA, Billerbeck AE, Madureira G, Arnhold IJ, Medeiros MA, Marcondes JA, Longui CA, Nicolau W, Bloise W, Mendonca BB. Low frequency of CYP2B deletions in Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylas deficiency. Hum Hered. 1999 Jan;49(1):9–14. doi: 10.1159/000022833. PMID: 10189236.
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date	199901
identifier	https://pubmed.ncbi.nlm.nih.gov/10189236 https://doi.org/10.1159/000022833
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
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Total number of triples: 50.