Chromosomal abnormalities in 163 Tunisian couples with recurrent miscarriages

por Ayed, Wiem, Messaoudi, Islem, Belghith, Zouhour, Hammami, Wajih, Chemkhi, Imen, Abidli, Nabila, Guermani, Helmy, Obay, Rim, Amouri, Ahlem
Publicado 2017

Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome

por Ben Haj Ali, Abir, Amouri, Ahlem, Sayeb, Marwa, Makni, Saloua, Hammami, Wajih, Naouali, Chokri, Dallali, Hamza, Romdhane, Lilia, Bashamboo, Anu, McElreavey, Kenneth, Abdelhak, Sonia, Messaoud, Olfa
Publicado 2019