Cutis Aplasia as a Clinical Hallmark for the Syndrome Associated with 19Q13.11 Deletion: the Possible Role for Uba2 Gene

AuthID
 P-00A-CEH
5
Author(s)
Estevinho, A
·
Tipo de Documento
Article
Year published
2015
Publicado
in MOLECULAR CYTOGENETICS, ISSN: 1755-8166
Volume: 8, Número: 1
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Wos®
Scopus®
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Publication Identifiers
SCOPUS: 2-s2.0-84927942449
Wos: WOS:000353015200001
Source Identifiers
ISSN: 1755-8166
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