English
 
User Manual Privacy Policy Disclaimer Contact us
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  Whole-exome sequencing for finding de novo mutations in sporadic mental retardation

Robinson, P. N. (2010). Whole-exome sequencing for finding de novo mutations in sporadic mental retardation. Genome Biology, 11(12), 11:144-11:144. doi:10.1186/gb-2010-11-12-144.

Item is

Basic

show hide
Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0010-79BF-B Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0010-79C0-5
Genre: Journal Article
Alternative Title : Genome Biol

Files

show Files
hide Files
:
gb-2010-11-12-144.pdf (Any fulltext), 284KB
 
File Permalink:
-
Name:
gb-2010-11-12-144.pdf
Description:
-
Visibility:
Restricted (Max Planck Institute for Molecular Genetics, Berlin; )
MIME-Type / Checksum:
application/pdf
Technical Metadata:
Copyright Date:
-
Copyright Info:
eDoc_access: MPG
License:
-

Locators

show

Creators

show
hide
 Creators:
Robinson, P. N.1, Author              
Affiliations:
1Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433557              

Content

show
hide
Free keywords: -
 Abstract: Recent work has used a family-based approach and whole-exome sequencing to identify de novo mutations in sporadic cases of mental retardation.

Details

show
hide
Language(s): eng - English
 Dates: 2010-12-21
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: -
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Genome Biology
  Alternative Title : Genome Biol
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 11 (12) Sequence Number: - Start / End Page: 11:144 - 11:144 Identifier: ISSN: 1465-6906