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- W2015447639 abstract "We report on a patient with severe psychomotor disability, numerous dysmorphic features, and congenital malformations resulting from a complex genomic rearrangement on 16q24.1‐q24.3 involving a de novo duplication‐triplication pattern. To the best of our knowledge, this is the first reported patient presenting with this aberration within the distal chromosome 16q. We suggest that the clinical phenotype of our patient results from over‐dosage of genes mapped to the region with duplication/triplication (five genes: FOXF1 , FOXC2 , ANKRD11 , SPG7 and FANCA seem to play a peculiar role). Detailed molecular characterization and documentation of the complex genomic rearrangement observed in the proband and of the clinical presentation are important for accurate genotype‐phenotype correlations in genetic counseling. Delineation of the gene map for the terminal region of chromosome 16q will provide insight into this chromosome 16q24.1‐q24.3 contiguous gene duplication‐triplication syndrome. © 2014 Wiley Periodicals, Inc." @default.
- W2015447639 created "2016-06-24" @default.
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- W2015447639 date "2014-08-08" @default.
- W2015447639 modified "2023-10-18" @default.
- W2015447639 title "The first case of a patient with de novo partial distal 16q tetrasomy and a data's review" @default.
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- W2015447639 doi "https://doi.org/10.1002/ajmg.a.36686" @default.
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