Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes

Congenital Anomalies,Volume 0, Issue ja, -Not available-.

Source: Congenital Anomalies - September 18, 2018 Category: Genetics & Stem Cells Authors: Jorge Rom án Corona‐Rivera , Alfredo Corona‐Rivera , Luz Consuelo Zepeda‐Romero , Izabel Maryalexandra Rios‐Flores , Jehú Rivera‐Vargas , Mireya Orozco‐Vela , Uriel Francisco Santana‐Bejarano , Elizabeth Torres� Source Type: research