A 3,195 Kb Duplication at 2Q14.3 in a Proband with a T(17;19)(P13.1;P13.3)Mat Is Most Likely Associated with Craniofacial Dimorphisms, Developmental and Neurological Anomalies

AuthID
 P-00W-HKP
7
Author(s)
Marques, M
·
Mota-Freitas, M
·
Candeias, C
·
Fortuna, A
·
David, D
Document Type
Abstract
Year published
2022
Published
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 30, Issue: SUPPL 1, Pages: 358-359 (2)
Indexing
Wos®
Publication Identifiers
Wos: WOS:000779367701406
Source Identifiers
ISSN: 1018-4813
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