CORE
🇺🇦Â
 make metadata, not war
Services
Research
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Search for <em>ReCQL4</em> mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes
Authors
Aral B
Barlogis V
+48Â more
Baujat G
Baumann C
Bessis D
Blair E
Bodemer C
Boralevi F
Boute O
Brady AF
Callier P
Capra V
Collet C
Cordier MP
Cormier-Daire V
Coubes C
Courcet JB
Demeer B
DiDonato N
Elalaoui SC
Faivre L
Francannet C
Franques J
Gauthier S
Genevieve D
Gigot N
Goldenberg A
Gonzalez-Ensenat MA
Holder-Espinasse M
Martorell L
Megarbane A
Moldovan O
Parent P
Pasquier L
Philip N
Piard J
Pierquin G
Puzenat E
Rio M
Riviere JB
Rodriguez A
Sousa AB
Sznajer Y
Tajir M
Tardieu M
Thauvin-Robinet C
Thevenon J
Toutain A
Vabres P
Wright M
Publication date
Publisher
Wiley-Blackwell
Abstract
Abstract is not available.
Similar works
Full text
Available Versions
Newcastle University E-Prints
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:eprints.ncl.ac.uk:212053
Last time updated on 30/05/2021