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
·
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
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Wos®
Publication Identifiers
Wos: WOS:000480733400163
Source Identifiers
ISSN: 0025-7974
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