Melo, J. B., Estevinho, A., Saraiva, J., Ramos, L., & Carreira, I. M. (2015). Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: The possible role for UBA2 gene.
Chicago Style CitationMelo, Joana B., Alexandra Estevinho, Jorge Saraiva, Lina Ramos, and Isabel M. Carreira. Cutis Aplasia As a Clinical Hallmark for the Syndrome Associated With 19q13.11 Deletion: The Possible Role for UBA2 Gene. 2015.
MLA CitationMelo, Joana B., et al. Cutis Aplasia As a Clinical Hallmark for the Syndrome Associated With 19q13.11 Deletion: The Possible Role for UBA2 Gene. 2015.
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