Title:

A Common Molecular Mechanism Underlies Two Phenotypically Distinct 17p13.1 Microdeletion Syndromes

Author:

Adam Shlien,Berivan Baskin,Maria Isabel W. Achatz,Dimitrios J. Stavropoulos,Kim E. Nichols,Louanne Hudgins,Chantal F. Morel,Margaret P. Adam,Nataliya Zhukova,Lianne Rotin,Ana Novokmet,Harriet Druker,Mary Shago,Peter N. Ray,Pierre Hainaut,David Malkin

Publication:

The American Journal of Human Genetics

Publisher:

Elsevier

Date:

12 November 2010

Copyright © 2010, Elsevier

 User ID  
 
 Password  
 
 Enable Auto Login
Forgot Password/User ID?
If you're a copyright.com user, you can login to RightsLink using your copyright.com credentials.
Already a RightsLink user or want to learn more?

Welcome to RightsLink

Elsevier has partnered with Copyright Clearance Center's RightsLink service to offer a variety of options for reusing Elsevier content. Select the "I would like to ..." drop-down menu to view the many reuse options available to you.

I would like to...

 


To request permission for a type of use not listed, please contact Elsevier Global Rights Department.

Are you the author of this Elsevier journal article?

 

Copyright © 2014 Copyright Clearance Center, Inc. All Rights Reserved. Privacy statement.
Comments? We would like to hear from you. E-mail us at customercare@copyright.com