21-Hydroxylase Deficiency - A Bibliography and Dictionary by Philip M. Parker

By Philip M. Parker

In March 2001, the nationwide Institutes of future health issued the subsequent caution: "The variety of sites supplying health-related assets grows on a daily basis. Many websites offer necessary info, whereas others can have details that's unreliable or misleading." moreover, as a result swift raise in Internet-based details, many hours will be wasted looking out, deciding upon, and printing. when you consider that basically the smallest fraction of knowledge facing 21-hydroxylase deficiency is listed in se's, resembling www.google.com or others, a non-systematic method of net study could be not just time eating, but additionally incomplete. This e-book used to be created for doctors, scholars, and participants of most of the people who are looking to behavior scientific study utilizing the main complicated instruments on hand and spending the smallest amount of time doing so.

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Extra resources for 21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16798278&query_hl=4&itool=pubmed_docsum • Nonclassic 21-hydroxylase deficiency. Author(s): Dewailly D. Source: Seminars in Reproductive Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12428204&query_hl=4&itool=pubmed_docsum • Nonclassic adrenal hyperplasia due to 21-hydroxylase deficiency. Author(s): Drucker S, New MI. Source: Pediatric Clinics of North America. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=3302893&query_hl=4&itool=pubmed_docsum • Non-classical 21-hydroxylase deficiency in children: association of adrenocorticotropic hormone-stimulated 17-hydroxyprogesterone with the risk of compound heterozygosity with severe mutations.

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.

Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=8055790&query_hl=4&itool=pubmed_docsum • Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21hydroxylase deficiency. Author(s): Witchel SF, Lee PA, Suda-Hartman M, Trucco M, Hoffman EP. Source: The Journal of Clinical Endocrinology and Metabolism. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=9215278&query_hl=4&itool=pubmed_docsum • Evidence for frequent gene conversion in the steroid 21-hydroxylase P-450(C21) gene: implications for steroid 21-hydroxylase deficiency.

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