Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

por Sbiti, Aziza, El Kerch, Fatiha, Sefiani, Abdelaziz
Publicado 2002

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report

por Amasdl, Saadia, Natiq, Abdelhafid, Elalaoui, Siham Chafai, Sbiti, Aziza, Liehr, Thomas, Sefiani, Abdelaziz
Publicado 2016

Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome

por BAZIZ, Meriem, HAMOULI-SAID, Zohra, RATBI, Ilham, HABEL, Mohamed, GUAOUA, Soukaina, SBITI, Aziza, SEFIANI, Abdelaziz
Publicado 2016

15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review

por Benbouchta, Yahya, De Leeuw, Nicole, Amasdl, Saadia, Sbiti, Aziza, Smeets, Dominique, Sadki, Khalid, Sefiani, Abdelaziz
Publicado 2021

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature

por Amasdl, Saadia, Natiq, Abdelhafid, Sbiti, Aziza, Zerkaoui, Maria, Lyahyai, Jaber, Amzazi, Saaid, Liehr, Thomas, Sefiani, Abdelaziz
Publicado 2016

Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia

por Doubaj, Yassamine, Zrhidri, Abdelali, Elalaoui, Siham Chafai, Lyahyai, Jaber, El Kadiri, Youssef, Elkassimi, Nadia, Sbiti, Aziza, El Kababri, Maria, Hessissen, Laila, Sefiani, Abdelaziz
Publicado 2021