Detection of Copy Number Variations in Rare Mendelian Disorders Using Whole Exome Sequencing

AuthID
 P-00Q-ZHN
9
Author(s)
Barbosa, S
·
Lopes, A
·
Arinto, P
·
Tipo de Documento
Abstract
Year published
2019
Publicado
in MEDICINE, ISSN: 0025-7974
Volume: 98, Número: 26
Conference
22Nd Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 15-17, 2018, Location: Porto, PORTUGAL, Patrocinadores: Portuguese Soc Human Genet
Indexing
Wos®
Publication Identifiers
Wos: WOS:000480733400163
Source Identifiers
ISSN: 0025-7974
Export Publication Metadata
Lista Marked
 Adicionar à lista Marked
Info
At this moment we don't have any links to full text documens.

Um espaço para investigadores e suas Instituições

Links Úteis

Ajuda

© 2024 CRACS & Inesc TEC - All Rights Reserved Política de Privacidade | Terms of Service