Abstract
A case of 12p13.2 heterozygous gene deletion syndrome: congenital thrombocytopenia, ectrodactyly, and tooth deformities
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https://doi.org/10.3760/cma.j.issn.0253-2727.2021.11.014
Journal: Chinese Journal of Hematology | Publication Date: Nov 1, 2021 |
License type: CC BY |
A case of 12p13.2 heterozygous gene deletion syndrome: congenital thrombocytopenia, ectrodactyly, and tooth deformities
Join us for a 30 min session where you can share your feedback and ask us any queries you have