Vol 7: A new case of de novo 19p13.2p13.12 deletion in a girl with overgrowth and severe developmental delay.Reportar como inadecuado



 Vol 7: A new case of de novo 19p13.2p13.12 deletion in a girl with overgrowth and severe developmental delay.


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This article is from Molecular Cytogenetics, volume 7.AbstractBackground: We report clinical and molecular cytogenetic characterization of a 2 year-old girl with 19p13.2p13.12 microdeletion and compare her clinical features with those of three other patients reported before. Result: Array comparative genomic hybridization (aCGH) revealed in the pr

Autor: Natiq, Abdelhafid; Elalaoui, Siham Chafai; Miesch, Sevrine; Bonnet, Celine; Jonveaux, Philippe; Amzazi, Saaid; Sefiani, Abdelaziz

Fuente: https://archive.org/







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