Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene
Crossref DOI link: https://doi.org/10.1186/s13039-015-0123-x
Published Online: 2015-03-26
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Melo, Joana B
Estevinho, Alexandra
Saraiva, Jorge
Ramos, Lina
Carreira, Isabel M
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