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

By Philip M. Parker

In March 2001, the nationwide Institutes of wellbeing and fitness issued the next caution: "The variety of sites providing health-related assets grows on a daily basis. Many websites supply important details, whereas others could have details that's unreliable or misleading." in addition, as a result speedy raise in Internet-based details, many hours could be wasted looking, picking, and printing. due to the fact 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 net learn should 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 learn utilizing the main complex 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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Author(s): Chrousos GP, Loriaux DL, Mann DL, Cutler GB Jr. Source: Annals of Internal Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=6977282&query_hl=4&itool=pubmed_docsum • Late-onset 21-hydroxylase deficiency. Author(s): Chrousos GP, Munabi A, Cutler GB Jr, Loriaux DL. Source: Annals of Internal Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=6285788&query_hl=4&itool=pubmed_docsum • Late-onset 21-hydroxylase deficiency: reliable diagnosis by steroid analysis of random urine collections.

Author(s): Balkin MS, Altchek A. Source: J Reprod Med. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=3488399&query_hl=4&itool=pubmed_docsum 38 21-Hydroxylase Deficiency • Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations. Author(s): Chrousos GP, Loriaux DL, Mann D, Cutler GB Jr. Source: Hormone Research. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=6290362&query_hl=4&itool=pubmed_docsum • Late-onset 21-hydroxylase deficiency mimicking idiopathic hirsutism or polycystic ovarian disease.

Author(s): Parenteau C, Mongeau CJ, Benard B, Maheux P. Source: Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11421542&query_hl=4&itool=pubmed_docsum • Pitfall of newborn screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Author(s): Rohrer TR, Gassmann KF, Pavel ME, Dorr HG. Source: Biology of the Neonate. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=12566686&query_hl=4&itool=pubmed_docsum • Pitfalls of PCR-based genotyping in patients with 21-hydroxylase deficiency.

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