Duplication of the Rubinstein-Taybi region on 16p13.3 is associated with a distinctive phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference13 articles.
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2. Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region;Berg;Genet Med,2007
3. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13;de Ravel;Eur J Med Genet,2005
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2. Clinical outcomes of fetuses with chromosome 16 short arm copy number variants;Molecular Genetics & Genomic Medicine;2023-04-04
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4. An Indian infant with de novo duplication of 16p chromosome: A rare genetic syndrome;Indian Journal of Medical Sciences;2020-12-22
5. De novo 16p13.3-p12.3 duplication in a child with syndromic developmental delay;Gene Reports;2020-09
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