Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency-Reference-Cited by-同舟云学术

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Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Published:2007-04 Issue:4 Volume:90 Page:414-421
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Wilson Robert C.,Nimkarn Saroj,Dumic Miro,Obeid Jihad,Azar Maryam,Najmabadi Hossein,Saffari Fatemeh,New Maria I.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference52 articles.

1. Molecular cloning of steroid 21-hydroxylase;White;Ann. N. Y. Acad. Sci.,1985

2. Structure of the human steroid 21-hydroxylase genes;White;Proc. Natl. Acad. Sci. USA,1986

3. Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene;Higashi;Proc. Natl. Acad. Sci. USA,1986

4. Adult height and fertility in men with congenital virilizing adrenal hyperplasia;Urban;N. Engl. J. Med.,1978

5. Steroidogenic enzyme activities, morphology, and receptor studies of a testicular adrenal rest in a patient with congenital adrenal hyperplasia;Clark;J. Clin. Endocrinol. Metab.,1990

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2. A MinION-based Long-Read Sequencing Application With One-Step PCR for the Genetic Diagnosis of 21-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2023-10-06

3. The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population;Frontiers in Endocrinology;2023-05-31

4. Genotype-phenotype correlation in patients with 21-hydroxylase deficiency;Frontiers in Endocrinology;2023-03-13

5. Clinical analysis of 78 patients with nonclassical 21-hydroxylase deficiency;Archives of Gynecology and Obstetrics;2023-02-11

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