Seminiferous tubule function in delayed-onset X-linked adrenal hypoplasia congenita associated with incomplete hypogonadotrophic hypogonadism-Reference-Cited by-同舟云学术

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Seminiferous tubule function in delayed-onset X-linked adrenal hypoplasia congenita associated with incomplete hypogonadotrophic hypogonadism

Published:2007-09-04 Issue:0 Volume:0 Page:070907134102005-???
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Bergadá Ignacio,Andreone Luz,Bedecarrás Patricia,Ropelato María Gabriela,Copelli Silvia,Laissue Paul,Rey Rodolfo A.,Campo Stella

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.2007.03026.x/fullpdf

Reference42 articles.

1. A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal

2. Clinical and Functional Effects of Mutations in the DAX-1 Gene in Patients with Adrenal Hypoplasia Congenita

3. The Role of DAX-1 in Reproduction

4. A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism

5. Three Novel Mutations and a De Novo Deletion Mutation of the DAX-1 Gene in Patients with X-Linked Adrenal Hypoplasia Congenita

Cited by 15 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. Adult‑onset X‑linked adrenal hypoplasia congenita caused by a novel mutation in DAX1/NR0B1: A case report and literature review;Experimental and Therapeutic Medicine;2022-08-19

2. Effect of Recombinant Gonadotropin on Testicular Function and Testicular Sperm Extraction in Five Cases of NR0B1 (DAX1) Pathogenic Variants;Frontiers in Endocrinology;2022-03-30

3. Biomarkers of male hypogonadism in childhood and adolescence;Advances in Laboratory Medicine / Avances en Medicina de Laboratorio;2020-06-25

4. Genetic Evaluation of Patients With Delayed Puberty and Congenital Hypogonadotropic Hypogonadism: Is it Worthy of Consideration?;Frontiers in Endocrinology;2020-05-19

5. GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing;European Journal of Endocrinology;2018-03

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