Pediatric M5 acute myeloid leukemia with MLL-SEPT6 fusion and a favorable outcome

por Chebly, Alain, Djambas Khayat, Claudia, Yammine, Tony, Korban, Rima, Semaan, Warde, Bou Zeid, Jessica, Farra, Chantal
Publicado 2021

Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variants

por Daou, Melissa, Souaid, Mirna, Yammine, Tony, Khneisser, Issam, Mansour, Hicham, Salem, Nabiha, Nemr, Antony, Awwad, Johnny, Moukarzel, Adib, Farra, Chantal
Publicado 2023

A rare case of acute myeloid leukemia with t(12;19)(q13;q13)

por Chebly, Alain, Haddad, Fady Gh, Bassil, Josiane, Yammine, Tony, Korban, Rima, Semaan, Warde, El Karak, Fady, Kourie, Hampig Raphael, Farra, Chantal
Publicado 2020

PI4K2A deficiency causes innate error in intracellular trafficking with developmental and epileptic‐dyskinetic encephalopathy

por Dafsari, Hormos Salimi, Pemberton, Joshua G., Ferrer, Elizabeth A., Yammine, Tony, Farra, Chantal, Mohammadi, Mohammad Hasan, Ghayoor Karimiani, Ehsan, Hashemi, Narges, Souaid, Mirna, Sabbagh, Sandra, Najarzadeh Torbati, Paria, Khan, Suliman, Roze, Emmanuel, Moreno‐De‐Luca, Andres, Bertoli‐Avella, Aida M., Houlden, Henry, Balla, Tamas, Maroofian, Reza
Publicado 2022