Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas-Reference-Cited by-同舟云学术

Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas

Published:2002-06 Issue:6 Volume:56 Page:811-816
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:

Author:

Baumgartner-Parzer S. M.,Pauschenwein S.,Waldhäusl W.,Pölzler K.,Nowotny P.,Vierhapper H.

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2002.01299.x/fullpdf

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3. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease;Blanchong;Journal of Experimental Medicine,2000

4. Adrenal mass;Cook;Endocrinology and Metabolism Clinics of North America,1997

5. Genotyping of CYP21, linked chromosome 6p Markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia;Fitness;Journal of Clinical Endocrinology and Metabolism,1999

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