First Familial Case of 16P13.3 Microdeletion Syndrome - Two New Cases Illustrating the Phenotype of This Recently Described Syndrome

AuthID
 P-018-GXS
6
Author(s)
Macedo, C
·
Sá, MSE
·
Monteiro, JP
·
Sousa, A
·
Sousa, AB
Document Type
Abstract
Year published
2024
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 32, Pages: 1119-1120 (2)
Indexing
Wos®
Publication Identifiers
Wos: WOS:001421430500883
Source Identifiers
ISSN: 1018-4813
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