Juan Antonio Bafallíu

Intrachromosomal partial triplication of chromosome 13 secondary to a paternal duplication with mild phenotypic effect

Juan Antonio Bafallíu, Mònica Santos, Carme Fuster et al. · American Journal of Medical Genetics Part A · 2008 · 76 citations

Life Sciences, Genetics, Molecular Genetics +13

Clinical comparison of 10q26 overlapping deletions: Delineating the critical region for urogenital anomalies

Ascensión Vera‐Carbonell, Vanesa López‐González, Juan Antonio Bafallíu et al. · American Journal of Medical Genetics Part A · 2015 · 58 citations

Life Sciences, Genetics, Molecular Genetics +17

Prenatal diagnosis of <i>de novo</i> deletions of 8p23.1 or 15q26.1 in two fetuses with diaphragmatic hernia and congenital heart defects

I. López, Juan Antonio Bafallíu, Maldonado Bernabé et al. · Prenatal Diagnosis · 2006 · 39 citations

Medicine, Genetics, Molecular Genetics +17

Pre‐ and postnatal findings in a patient with a novel rec(8)dup(8q)inv(8)(p23.2q22.3) associated with san luis valley syndrome

Ascensión Vera‐Carbonell, Vanesa López‐González, Juan Antonio Bafallíu et al. · American Journal of Medical Genetics Part A · 2013 · 38 citations

Life Sciences, Genetics, Molecular Genetics +14

Rapp–Hodgkin syndrome and SHFM1 patients: Delineating the p63–Dlx5/Dlx6 pathway

Ascensión Vera‐Carbonell, María Rosa Moya‐Quiles, María Juliana Ballesta‐Martínez et al. · Gene · 2012 · 18 citations

Medicine, Oncology, Pathology +6