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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 Report of a Saudi BoyAl-Hassnan, Zuhair N.,Al-Qattan, Mohammad M.,Alsufayan, Faris A. S.,Jarman, Abdulaziz,Mahabbat, Nehal,Rafique, Atif,Rahbeeni, Zuhair A.
Beh？et Disease-Like Symptoms with a Novel COPA MutationAnderson, E.,Cardinal, J.,Coman, D.,Hatch, J.,Langguth, D.
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