46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters-Reference-Cited by-同舟云学术

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46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters

Published:2023-06 Issue: Volume: Page:
ISSN:0003-4266
Container-title:Annales d'Endocrinologie
language:en
Short-container-title:Annales d'Endocrinologie

Author:

Yami channaiah Chethan,Memon Saba Samad,Sarathi Vijaya,Lila Anurag Ranjan^ORCID,Barnabas Rohit,Raghav Darpan,Bhandare Vishwambhar V.,Arya Sneha,Thakkar Hemangini,Patil Virendra Ashokrao,Karlekar Manjiri,Kunwar Ambarish,Bandgar Tushar

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

Reference43 articles.

1. Organization of the human aromatase p450 (CYP19) gene;Bulun;Semin Reprod Med,2004

2. A new cause of female pseudohermaphroditism: placental aromatase deficiency;Shozu;J Clin Endocrinol Metab,1991

3. Genetic and clinical spectrum of aromatase deficiency in infancy, childhood and adolescence;Belgorosky;Horm Res Paediatr,2009

4. Aromatase and estrogen receptor α deficiency;Bulun;Fertil Steril,2014

5. Five new cases of 46,XX aromatase deficiency: clinical follow-up from birth to puberty, a novel mutation, and a founder effect;Marino;J Clin Endocrinol Metab,2015

Cited by 1 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. Long-term outcomes in non-CAH 46,XX DSD;Frontiers in Endocrinology;2024-04-30

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