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Publications
Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene
Publication with shared reference
10.1186/s13039-015-0123-x
Home
Publications
Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene
Publication with shared reference
10.1186/s13039-015-0123-x
Publications with shared reference:
Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene
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