檢索結果 - Mahabbat, Nehal
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Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein–Taybi Syndrome Phenotype: A Case... 由 Al-Qattan, Mohammad M., Rahbeeni, Zuhair A., Al-Hassnan, Zuhair N., Jarman, Abdulaziz, Rafique, Atif, Mahabbat, Nehal, Alsufayan, Faris A. S.
出版 2020Text -
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