Implications of CYP21A2 gene duplications in carrier screening and prenatal diagnosis of congenital adrenal hyperplasia due to 21 Hydroxylase deficiency-Reference-Cited by-同舟云学术

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Implications of CYP21A2 gene duplications in carrier screening and prenatal diagnosis of congenital adrenal hyperplasia due to 21 Hydroxylase deficiency

Published:2022 Issue:1 Volume:2 Page:47
ISSN:2772-5170
Container-title:Indian Pediatrics Case Reports
language:en
Short-container-title:Indian Pediatr Case Rep

Author:

Dubey Sudhisha,Saxena Renu,Puri RatnaDua,Verma IshwarChander

Publisher

Medknow

Reference11 articles.

1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr Rev,2000

2. Newborn screening for congenital adrenal hyperplasia;Therrell;Endocrinol Metab Clin North Am,2001

3. Newborn screening for congenital hypothyroidism and congenital adrenal hyperplasia;ICMR;Indian J Pediatr,2018

4. Genetics of congenital adrenal hyperplasia;Hannah-Shmouni;Endocrinol Metab Clin North Am,2017

5. Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort;Krone;J Clin Endocrinol Metab,2013

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