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|Title:||A de novo interstitial 6q deletion in a boy with a split hand malformation|
|Abstract:||We report on a de novo interstitial deletion of (6)(q15q22.2) in a 5-year-old boy with developmental delay, microcephaly, facial dysmorphism, cryptorchidism, congenital heart defect, and split-hand malformation. Previous reports and this patient suggest that 6q21 may contain a gene or genes related either directly or indirectly to limb development.|
|Appears in Collections:||Producción científica UdeG (prueba)|
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