Home  |   Archive  |   Online Submission  |   News & Events  |   Subscribe  |   APFA  |   Society  |   Contact Us  |   中文版
Search   
 
Journal

-Ahead of print
-Authors' Accepted
    Manuscripts
new!
-Current Issue
-Archive
-Acknowledgments
-Special Issues
-Browse by Category

Manuscript Submission

-Online Submission
-Online Review
-Instruction for Authors
-Instruction for Reviewers
-English Corner new!

About AJA

-About AJA
-Editorial Board
-Contact Us
-News

Resources & Services

-Advertisement
-Subscription
-Email alert
-Proceedings
-Reprints

Download area

-Copyright licence
-EndNote style file
-Manuscript word template
-Guidance for AJA figures
    preparation (in English)

-Guidance for AJA figures
    preparation (in Chinese)

-Proof-reading for the
    authors

-AJA Club (in English)
-AJA Club (in Chinese)

 
Abstract

Volume 13, Issue 2 (March 2011) 13, 203–204; 10.1038/aja.2010.115

Copy number variation associated with Kallmann syndrome: new genetics insights from genome-wide studies

Ericka B Trarbach

Unity of Endocrinology—LIM25 and LIM42, Faculty of Medicine, University of Sao Paulo, 01246-903 Sao Paulo, Brazil

Correspondence: Dr EB Trarbach, (trarbach@hotmail.com)

Advance online publication 1 March 2011

Abstract

No abstract available

PDF |

 
Browse:  4095
 
Asian Journal of Andrology CN 31-1795/R ISSN 1008-682X  Copyright © 2023  Shanghai Materia Medica, Chinese Academy of Sciences.  All rights reserved.