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 Boy. - Document
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Chromosome 16 - Wikipedia
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M M Al-Qattan's research works King Saud University, Riyadh (KKUH) and other places
M M Al-Qattan's research works King Saud University, Riyadh (KKUH) and other places
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PDF) Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: A case report
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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 Boy. - Document
Clinical outcomes of fetuses with chromosome 16 short arm copy number variants - Kang - 2023 - Molecular Genetics & Genomic Medicine - Wiley Online Library