1. 16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations. Issue 5 (4th October 2018) Authors: Allach El Khattabi, Laïla; Heide, Solveig; Caberg, Jean-Hubert; Andrieux, Joris; Doco Fenzy, Martine; Vincent-Delorme, Caroline; Callier, Patrick; Chantot-Bastaraud, Sandra; Afenjar, Alexandra; Boute-Benejean, Odile; Cordier, Marie Pierre; Faivre, Laurence; Francannet, Christine; Gerard, Marion; ... Journal: Journal of medical genetics Issue: Volume 57:Issue 5(2020) Page Start: 301 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature. (December 2016) Authors: Amasdl, Saadia; Natiq, Abdelhafid; Sbiti, Aziza; Zerkaoui, Maria; Lyahyai, Jaber; Amzazi, Saaid; Liehr, Thomas; Sefiani, Abdelaziz Journal: BMC research notes Issue: Volume 9:Number 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability. (3rd September 2022) Authors: EL Amrani, Zhour; Elalaoui, Siham Chafai; Jdioui, Wafae; Sbiti, Aziza; Ratbi, Ilham; Liehr, Thomas; Sefiani, Abdelaziz; Natiq, Abdelhafid Journal: Ophthalmic genetics Issue: Volume 43:Number 5(2022) Page Start: 689 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion. Issue 1 (12th November 2016) Authors: Natiq, Abdelhafid; Lysy, Philippe A.; Gillemans, Nynke; Schaap, Rianne; Sefiani, Abdelaziz; Amzazi, Saaid; Chafai El‐Alaoui, Siham; Cantú, Ileana; Banjanin, Bella; van Lom, Kirsten; Harteveld, Cornelis L.; Philipsen, Sjaak Journal: American journal of hematology Issue: Volume 92:Issue 1(2017:Jan.) Page Start: E2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report. (December 2016) Authors: Amasdl, Saadia; Natiq, Abdelhafid; Elalaoui, Siham; Sbiti, Aziza; Liehr, Thomas; Sefiani, Abdelaziz Journal: Journal of medical case reports Issue: Volume 10:Number 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma. (2020) Authors: Hamdaoui, Hasna; Natiq, Abdelhafid; Benlarroubia, Oumaima; Liehr, Thomas; Dehbi, Hind; Loukhmas, Latifa; Chegdani, Fatima Journal: Leukemia research reports Issue: Volume 14(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder. (19th March 2007) Authors: Ouldim, Karim; Natiq, Abdelhafid; Jonveaux, Philippe; Sefiani, Abdelaziz Other Names: Fellous Marc Academic Editor. Journal: Journal of biomedicine and biotechnology Issue: Volume 2007(2007) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗