Saadia Amasdl

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

T. Liehr, J. Lyahyai, A. Sbiti, 2016, BMC Research Notes.

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

N. de Leeuw, D. Smeets, A. Sbiti, 2020, Italian Journal of Pediatrics.

Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness

D. Sanlaville, A. Sbiti, A. Sefiani, 2017, Cytogenetic and Genome Research.

11p13 Deletion Syndrome: First Case in Morocco Detected by FISH

T. Liehr, B. Meyer, A. Sefiani, 2014 .

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

T. Liehr, S. Elalaoui, A. Sbiti, 2016, Journal of Medical Case Reports.

Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease

L. Raymond, J. Lyahyai, A. Sefiani, 2017, Pediatric Rheumatology.

High frequency of hotspot mutation in PTPN11 gene among Moroccan patients with Noonan syndrome.

J. Lyahyai, A. Sefiani, I. Ratbi, 2023, Journal of applied genetics.