Clinical and molecular characterization of maturity onset-diabetes of the young caused by hepatocyte nuclear factor-4 alpha mutation: red flags for prediction of the diagnosis

por Mohamed, Sarar, Elkholy, Susan, El-Meleagy, Ebtessam, Abu-Amero, Khaled, Hellani, Ali M.
Publicado 2014

Chromosome 6 microdeletion in a patient with syndromic congenital cranial dysinnervation disorder

por Abu-Amero, Khaled K., Kondkar, Altaf A., Hellani, Ali M., Bosley, Thomas M., Khan, Arif O.
Publicado 2016

High-resolution analysis of DNA copy number alterations in patients with isolated sporadic keratoconus

por Abu-Amero, Khaled K., Hellani, Ali M., Al Mansouri, Sameer M., Kalantan, Hatem, Al-Muammar, Abdulrahman M.
Publicado 2011

A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation

por Abu-Amero, Khaled K, Hellani, Ali M, Salih, Mustafa A, Seidahmed, Mohammad Z, Elmalik, Tageldin S, Zidan, Ghassan, Bosley, Thomas M
Publicado 2010