1. A novel SOX18 mutation uncovered in Jordanian patient with hypotrichosis–lymphedema–telangiectasia syndrome by Whole Exome Sequencing. Issue 1 (February 2016) Authors: Bastaki, Fatma; Mohamed, Madiha; Nair, Pratibha; Saif, Fatima; Tawfiq, Nafisa; Al-Ali, Mahmoud Taleb; Brandau, Oliver; Hamzeh, Abdul Rezzak Journal: Molecular and cellular probes Issue: Volume 30:Issue 1(2016) Page Start: 18 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAE. Issue 1 (December 2017) Authors: Hamzeh, Abdul; Saif, Fatima; Nair, Pratibha; Binjab, Asma; Mohamed, Madiha; Al-Ali, Mahmoud; Bastaki, Fatma Journal: BMC pediatrics Issue: Volume 17:Issue 1(2017) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Characterization of an Emirati TMEM138 mutation leading to Joubert syndrome. Issue 1 (19th January 2017) Authors: Bizzari, Sami; Hamzeh, Abdul Rezzak; Nair, Pratibha; Mohamed, Madiha; Bastaki, Fatma Journal: Pediatrics international Issue: Volume 59:Issue 1(2017) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Characterization of an Emirati TMEM138 mutation leading to Joubert syndrome. Issue 1 (January 2017) Authors: Bizzari, Sami; Hamzeh, Abdul Rezzak; Nair, Pratibha; Mohamed, Madiha; Bastaki, Fatma Journal: Pediatrics international Issue: Volume 59:Issue 1(2017) Page Start: 113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases. Issue 6 (7th October 2018) Authors: Nair, Pratibha; Sabbagh, Sandra; Mansour, Hicham; Fawaz, Ali; Hmaimess, Ghassan; Noun, Peter; Dagher, Rawane; Megarbane, Hala; Hana, Sayeeda; Alame, Saada; Lamaa, Maher; Hasbini, Dana; Farah, Roula; Rajab, Mariam; Stora, Samantha; El‐Tourjuman, Oulfat; Abou Jaoude, Pauline; Chalouhi, Gihad; Sayad... Journal: Molecular genetics & genomic medicine Issue: Volume 6:Issue 6(2018) Page Start: 1041 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Evaluating the Impact of Outpatient Multi-Dose Medication Packaging Service (MDMPS) on Medication Adherence and Clinical Outcomes. (October 2020) Authors: Nair, Pratibha; Kee, Kok Wai; Mah, Choon Siong; Lee, Eng Sing Journal: Journal of primary care & community health Issue: Volume 11(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Genetics of multifactorial disorders: proceedings of the 6th Pan Arab Human Genetics Conference. Issue 1 (December 2016) Authors: Nair, Pratibha; Bizzari, Sami; Rajah, Nirmal; Assaf, Nada; Al-Ali, Mahmoud; Hamzeh, Abdul Journal: Journal of translational medicine Issue: Volume 14:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genomics into Healthcare: The 5th Pan Arab Human Genetics Conference and 2013 Golden Helix Symposium. Issue 5 (31st March 2014) Authors: Fortina, Paolo; Khaja, Najib Al; Ali, Mahmoud Taleb Al; Hamzeh, Abdul Rezzak; Nair, Pratibha; Innocenti, Federico; Patrinos, George P.; Kricka, Larry J. Journal: Human mutation Issue: Volume 35:Issue 5(2014:May) Page Start: 637 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Meta‐analyses of the association of HLA‐DRB1 alleles with rheumatoid arthritis among Arabs. (14th July 2016) Authors: Bizzari, Sami; Nair, Pratibha; Al Ali, Mahmoud Taleb; Hamzeh, Abdul Rezzak Journal: International journal of rheumatic diseases Issue: Volume 20:Number 7(2017) Page Start: 832 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Microcephalic primordial dwarfism in an Emirati patient with PNKP mutation. Issue 8 (27th May 2016) Authors: Nair, Pratibha; Hamzeh, Abdul Rezzak; Mohamed, Madiha; Saif, Fatima; Tawfiq, Nafisa; El Halik, Majdi; Al‐Ali, Mahmoud Taleb; Bastaki, Fatma Journal: American journal of medical genetics Issue: Volume 170:Issue 8(2016) Page Start: 2127 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗