Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency-Reference-Cited by-同舟云学术

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Low Frequency of CYP21B Deletions in Brazilian Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Published:1999 Issue:1 Volume:49 Page:9-14
ISSN:0001-5652
Container-title:Human Heredity
language:en
Short-container-title:Hum Hered

Author:

Bachega Tânia A.S.S.,Billerbeck Ana Elisa C.,Madureira Guiomar,Arnhold Ivo J.P.,Medeiros Maria A.,Marcondes José A.M.,Longui Carlos A.,Nicolau Willian,Bloise Walter,Mendonca Berenice B.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics

Cited by 30 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. 2+0 CYP21A2 deletion carrier — a limitation of the genetic testing and counseling: A case report;World Journal of Clinical Cases;2021-08-16

2. Molecular CYP21A2 diagnosis in 480 Brazilian patients with congenital adrenal hyperplasia before newborn screening introduction;European Journal of Endocrinology;2016-08

3. A Single Nucleotide Variant in the Promoter Region of 17β-HSD Type 5 Gene Influences External Genitalia Virilization in Females with 21-Hydroxylase Deficiency;Hormone Research in Paediatrics;2016

4. A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Gene;2013-09

5. CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia;Hormone and Metabolic Research;2013-01-15

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