Novel interstitial deletion in Xp22.3 in a typical X-linked recessive family with Kallmann syndrome-Reference-Cited by-同舟云学术

Novel interstitial deletion in Xp22.3 in a typical X-linked recessive family with Kallmann syndrome

Published:2018-02-14 Issue:4 Volume:50 Page:e12961
ISSN:0303-4569
Container-title:Andrologia
language:en
Short-container-title:Andrologia

Author:

Niu Y.¹²^ORCID,Zhou C.³⁴,Xu H.¹²,Wang D.¹²,Chen Y.¹²,Li Z.³⁴,Wang T.¹²,Pokhrel G.¹²,Wang D. W.³⁴,Liu J.¹²

Affiliation:

1. Department of Urology; Tongji Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan China

2. Institute of Urology; Tongji Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan China

3. Division of Cardiology; Department of Internal Medicine and Genetic Diagnosis Center; Tongji Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan China

4. Hubei Key Laboratory of Genetics and Molecular Mechanisms of Cardiological Disorders; Tongji Hospital; Tongji Medical College; Huazhong University of Science and Technology; Wuhan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/and.12961/fullpdf

Reference27 articles.

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3. Deletion analysis maps ocular albinism proximal to the steroid sulphatase locus;Bouloux;Clinical Genetics,1993