Fahed Halal

Haploinsufficiency of HDAC4 Causes Brachydactyly Mental Retardation Syndrome, with Brachydactyly Type E, Developmental Delays, and Behavioral Problems

Stephen R. Williams, Micheala A. Aldred, Vazken M. Der Kaloustian et al. · The American Journal of Human Genetics · 2010 · 297 citations · Full text

Genetic Disorder, Genetics, Developmental Delays +5

Frequency of the branchio‐oto‐renal (BOR) syndrome in children with profound hearing loss

F. Clarke Fraser, Johnson Sproule, Fahed Halal et al. · American Journal of Medical Genetics · 1980 · 258 citations

Neurotology, Early Diagnosis, Auditory Science +17

Autosomal dominant inheritance of the Kabuki make‐up (Niikawa‐Kuroki) syndrome

Fahed Halal, Robert B. Gledhill, Aaron Dudkiewicz · American Journal of Medical Genetics · 1989 · 96 citations

Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations

Nataliya Di Donato, Andreas Rump, Rainer Koenig et al. · European Journal of Human Genetics · 2013 · 90 citations · Full text

Rare Diseases, Actg1 Mutations, Mendelian Disorder +8

Acro‐renal‐ocular syndrome: Autosomal dominant thumb hypoplasia, renal ectopia, and eye defect

Fahed Halal, Magda Barsoum Homsy, Giiles Perreault · American Journal of Medical Genetics · 1984 · 80 citations