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1.
Clinical course of patients with nonclassical 21-hydroxylase deficiency (21-OHD) diagnosed in infancy and childhood.
Endocr J
; 55(2): 397-404, 2008 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-18385531
2.
Genetic analysis of Japanese patients with 21-hydroxylase deficiency: identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21.
J Clin Endocrinol Metab
; 87(6): 2668-73, 2002 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-12050231
3.
A highly specific heterologous enzyme immunoassay for 5 alpha-androstane-3 alpha, 17 beta-diol 17-glucuronide (androstanediol-17G) and developmental patterns of urinary androstanediol-17G excretions.
Steroids
; 67(3-4): 175-83, 2002 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-11856541
4.
Colon cancer in a 14-year-old female with turner syndrome: report of a case.
Dis Colon Rectum
; 46(11): 1560-2, 2003 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-14605580
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