Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review-Reference-Cited by-同舟云学术

Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review

Published:2022-09-30 Issue:6 Volume:97 Page:804-813
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Patil Virendra A.¹,Lila Anurag Ranjan¹^ORCID,Shah Nalini¹,Arya Sneha¹,Sarathi Vijaya²,Shah Ravikumar¹^ORCID,Jadhav Swati S.³^ORCID,Memon Saba Samad¹,Karlekar Manjiri¹,Bandgar Tushar¹^ORCID

Affiliation:

1. Department of Endocrinology Seth G S Medical College and KEM Hospital Mumbai Maharashtra India

2. Department of Endocrinology Vydehi Institute of Medical Sciences and Research Centre Bengaluru India

3. Sapthagiri Institute of Medical Sciences and Research Centre Bengaluru India

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14822

Reference22 articles.

1. European Consensus Statement on congenital hypogonadotropic hypogonadism—pathogenesis, diagnosis and treatment

2. Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice

3. GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing

4. Spectrum of phenotype and genotype of congenital isolated hypogonadotropic hypogonadism in Asian Indians

5. Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review

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