Whole Exome Sequencing- First Tier Test for Fetuses with Severe Central Nervous System Anomalies

AuthID
 P-018-DM0
11
Author(s)
Alves, C
·
Dias, C
·
Almeida, ML
·
Ramos, F
·
Pereira, N
·
Ramos, L
·
Reis Lima, M
Document Type
Abstract
Year published
2024
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 32, Pages: 1322-1322 (1)
Indexing
Wos®
Publication Identifiers
Wos: WOS:001407868901240
Source Identifiers
ISSN: 1018-4813
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