By Philip M. Parker
In March 2001, the nationwide Institutes of wellbeing and fitness issued the subsequent caution: "The variety of sites providing health-related assets grows on a daily basis. Many websites supply beneficial info, whereas others could have details that's unreliable or misleading." moreover, as a result quick bring up in Internet-based details, many hours could be wasted looking out, choosing, and printing. considering that merely the smallest fraction of data facing 21-hydroxylase deficiency is listed in se's, equivalent to www.google.com or others, a non-systematic method of web study could be not just time eating, but additionally incomplete. This publication was once created for doctors, scholars, and participants of most of the people who are looking to behavior clinical learn utilizing the main complicated instruments on hand and spending the smallest amount of time doing so.
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Extra info for 21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers
Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=2212957&query_hl=4&itool=pubmed_docsum Studies 33 • HLA family study in a group of Greek women with non-classical 21-hydroxylase deficiency. Author(s): Tertipi A, Papagrigoriou L, Kaldrimidis P, Gogou L, Dimou M, KoniaritouHagjicannaki K. Source: Hormone and Metabolic Research. Hormon- Und Stoffwechselforschung. Hormones Et Metabolisme. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8225196&query_hl=4&itool=pubmed_docsum • HLA-B14 and nonclassical 21-hydroxylase deficiency in a heterogeneous New York population.
Source: Obstetrics and Gynecology. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12738128&query_hl=4&itool=pubmed_docsum • Final height in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the Italian experience. Author(s): Brunelli VL, Russo G, Bertelloni S, Gargantini L, Balducci R, Chiesa L, Livieri C, De Sanctis C, Einaudi S, Virdis R, Saggese G, Chiumello G. Source: J Pediatr Endocrinol Metab. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12729404&query_hl=4&itool=pubmed_docsum Studies 27 • First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=6970799&query_hl=4&itool=pubmed_docsum • Longitudinal analysis of growth and puberty in 21-hydroxylase deficiency patients. Author(s): Van der Kamp HJ, Otten BJ, Buitenweg N, De Muinck Keizer-Schrama SM, Oostdijk W, Jansen M, Delemarre-de Waal HA, Vulsma T, Wit JM. Source: Archives of Disease in Childhood. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12138066&query_hl=4&itool=pubmed_docsum • Long-term follow-up of female patients with congenital adrenal hyperplasia from 21hydroxylase deficiency, with special emphasis on the results of vaginoplasty.
21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker