A New Mutation in Rpl10 Associated with X-Linked Syndromic Intellectual Disability in Two Families and Literature Review

AuthID
 P-00Q-ZFY
8
Author(s)
Venancio, M
·
Grote, L
·
Friez, M
·
Chanudet, E
·
Bachelli, C
·
Williams, H
·
Sousa, S
Document Type
Abstract
Year published
2019
Published
in MEDICINE, ISSN: 0025-7974
Volume: 98, Issue: 26
Conference
22Nd Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 15-17, 2018, Location: Porto, PORTUGAL, Sponsors: Portuguese Soc Human Genet
Indexing
Wos®
Publication Identifiers
Wos: WOS:000480733400151
Source Identifiers
ISSN: 0025-7974
Export Publication Metadata
Marked List
 Add to Marked List
Info
At this moment we don't have any links to full text documens.

A place for researchers and their institutions

Useful Links

Get Help

© 2024 CRACS & Inesc TEC - All Rights Reserved Privacy Policy | Terms of Service