1. An expansion of phenotype: novel homozygous variant in the MED17 identified in patients with progressive microcephaly and global developmental delay. (2nd October 2022) Authors: Rafiullah, Rafiullah; Albalawi, Alia M.; Alaradi, Sultan R.; Alluqmani, Majed; Mushtaq, Muhammad; Wali, Abdul; Basit, Sulman Journal: Journal of neurogenetics Issue: Volume 36:Number 4(2022) Page Start: 108 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Biallelic mutations in the LPAR6 gene causing autosomal recessive wooly hair/hypotrichosis phenotype in five Pakistani families. (11th May 2019) Authors: Khan, Ghulam M.; Hassan, Noor; Khan, Niamatullah; Humayun, Muhammad; Khan, Kafaitullah; Khaliq, Samira; Rehman, Fazal U.; Ahmed, Sheikh; Shah, Khadim; Khan, Sher A.; Muhammad, Noor; Wali, Abdul; Khan, Saadullah; Basit, Sulman; Ayub, Muhammad Journal: International journal of dermatology Issue: Volume 58:Number 8(2019) Page Start: 946 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Contracting out health services in fragile states. Issue 7543 (23rd March 2006) Authors: Palmer, Natasha; Strong, Lesley; Wali, Abdul; Sondorp, Egbert Journal: BMJ Issue: Volume 332:Issue 7543(2006) Page Start: 718 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Ethnobotanical and Biochemical Study of Berberis lycium Royle Collected from Different Areas of Azad Jammu and Kashmir. (26th September 2021) Authors: Fiaz Bukhari, Syeda Maria; Ali, Ghazanfar; Abbas, Syed Rizwan; Anjum, Zeeshan; Ahmed, Nasim; Munir, Ammara; Wali, Abdul; Ayub, Muhammad; Khan, Kafaitullah; Khames, Ahmed; Musthafa, Muneeb Muhamed Other Names: Ullah Riaz Academic Editor. Journal: Evidence-based complementary and alternative medicine Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic analysis of Xp22.3 micro-deletions in seventeen families segregating isolated form of X-linked ichthyosis. Issue 3 (December 2015) Authors: Ali, Raja Hussain; Mahmood, Sabba; Raza, Syed Irfan; Aziz, Abdul; Irfanullah, ; Naqvi, Syed Kamran-ul-Hassan; Wasif, Naveed; Ansar, Muhammad; Ahmad, Wasim; Shah, Sayed Hajan; Khan, Bakht Tarin; Zaman, Qaiser; Gul, Ajab; Wali, Abdul; Ali, Ghazanfar; Khan, Saadulah; Khisroon, Muhammad; Basit, Sulman Journal: Journal of dermatological science Issue: Volume 80:Issue 3(2015:Dec.) Page Start: 214 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome. (23rd February 2021) Authors: Ali, Ghazanfar; Sadia, ; Foo, Jia Nee; Nasir, Abdul; Chang, Chu-Hua; Chew, Elaine GuoYan; Latif, Zahid; Azeem, Zahid; Ain-ul-Batool, Syeda; Kazmi, Syed Akif Raza; Awan, Naheed Bashir; Khan, Abdul Hameed; Rehman, Fazal-Ur-; Khalid, Madiha; Wali, Abdul; Sarwar, Samina; Akhtar, Wasim; Ahmed Abbasi, ... Other Names: Erg n Sercan Academic Editor. Journal: BioMed research international Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular, Cytogenetic, and Hematological Analysis of Chronic Myeloid Leukemia Patients and Discovery of Two Novel Translocations. (13th August 2021) Authors: Asif, Muhammad; Hussain, Abrar; Wali, Abdul; Ahmed, Nazeer; Ali, Irfan; Iqbal, Zafar; Amir, Muhammad; Shafiq, Muhammad; Rasool, Mahmood Other Names: Urzua Ulises Academic Editor. Journal: Analytical cellular pathology Issue: Volume 2021(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Novel insertion and a previously reported nonsense variant of ALOXE3 gene lead to autosomal recessive ichthyosis in two Balochi families. (12th October 2018) Authors: Ijaz, Ambreen; Jelani, Musharraf; Panezai, Anila; Rabbani, Tahmina; Rasool, Iftikhar A.; Ahmad, Jamil; Wali, Abdul Journal: Congenital anomalies Issue: Volume 59:Number 5(2019) Page Start: 179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel missense alteration in LRP4 gene underlies Cenani–Lenz syndactyly syndrome in a consanguineous family. (3rd January 2020) Authors: Alrayes, Nuha; Aziz, Abdul; Ullah, Farman; Ishfaq, Muhammad; Jelani, Musharraf; Wali, Abdul Journal: Journal of gene medicine Issue: Volume 22:Number 1(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Principals' strategies for increasing students' participation in school leadership in a rural, mountainous region in Pakistan. (November 2020) Authors: Afzal Tajik, Mir; Wali, Abdul Journal: Improving schools Issue: Volume 23:Number 3(2020) Page Start: 245 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗