Tbl1Xr1 De Novo Deletion at 3(Q26.32) in a Boy with Developmental Delay, Growth Retardation and Dysmorphisms

AuthID
 P-013-C8D
5
Author(s)
Ferreira, SI
·
Val
·
Maia, S
·
Carreira, IM
Tipo de Documento
Abstract
Year published
2018
Publicado
in EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN: 1018-4813
Volume: 26, Páginas: 923-924 (2)
Indexing
Wos®
Publication Identifiers
Wos: WOS:000489312607222
Source Identifiers
ISSN: 1018-4813
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