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

By Philip M. Parker

ISBN-10: 0497112019

ISBN-13: 9780497112011

ISBN-10: 1429497335

ISBN-13: 9781429497336

In March 2001, the nationwide Institutes of health and wellbeing issued the subsequent caution: "The variety of websites providing health-related assets grows each day. Many websites supply helpful details, whereas others can have details that's unreliable or misleading." in addition, as a result quick raise in Internet-based info, many hours could be wasted looking out, deciding on, and printing. considering in simple terms the smallest fraction of knowledge facing 21-hydroxylase deficiency is listed in se's, equivalent to www.google.com or others, a non-systematic method of web learn may be not just time eating, but in addition incomplete. This ebook was once created for doctors, scholars, and individuals of most people who are looking to behavior scientific examine 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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Results of a multicenter study. Author(s): Hargitai G, Solyom J, Battelino T, Lebl J, Pribilincova Z, Hauspie R, Kovacs J, Waldhauser F, Frisch H; MEWPE-CAH Study Group. Source: Hormone Research. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11598369&query_hl=4&itool=pubmed_docsum • H28+C insertion in the CYP21 gene: a novel frameshift mutation in a Brazilian patient with the classical form of 21-hydroxylase deficiency. Author(s): Lau IF, Soardi FC, Lemos-Marini SH, Guerra Jr G Jr, Baptista MT, De Mello MP.

Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=7218273&query_hl=4&itool=pubmed_docsum • Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: a genetic study of Sardinian family. Author(s): Concolino P, Satta MA, Santonocito C, Carrozza C, Rocchetti S, Ameglio F, Giardina E, Zuppi C, Capoluongo E. Source: Clinica Chimica Acta; International Journal of Clinical Chemistry. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=16171792&query_hl=4&itool=pubmed_docsum • Location of the gene for 21-hydroxylase deficiency.

Source: Pediatric Research. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=6219334&query_hl=4&itool=pubmed_docsum • Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency. Author(s): Mornet E, Crete P, Kuttenn F, Raux-Demay MC, Boue J, White PC, Boue A. Source: American Journal of Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1985465&query_hl=4&itool=pubmed_docsum • Duplication of 111 bases in exon 1 of the CYP21 gene is combined with deletion of CYP21P-C4B genes in steroid 21-hydroxylase deficiency.

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21-Hydroxylase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker


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