1. A novel homozygous variant in BMPR1B underlies acromesomelic dysplasia Hunter–Thompson type. (10th January 2018) Authors: Ullah, Asmat; Umair, Muhammad; Muhammad, Dost; Bilal, Muhammad; Lee, Kwanghyuk; Leal, Suzanne M; Ahmad, Wasim Journal: Annals of human genetics Issue: Volume 82:Number 3(2018:May) Page Start: 129 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel homozygous variant in the SMOC1 gene underlying Waardenburg anophthalmia syndrome. (4th July 2017) Authors: Ullah, Asmat; Umair, Muhammad; Ahmad, Farooq; Muhammad, Dost; Basit, Sulman; Ahmad, Wasim Journal: Ophthalmic genetics Issue: Volume 38:Number 4(2017) Page Start: 335 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Foliar versus soil phosphorus (P) application for improving P use efficiency in wheat and maize in calcareous soils. (7th May 2021) Authors: , Rafiullah; Khan, Mohammad Jamal; Muhammad, Dost; Mussarat, Maria; , Huma; Adnan, Muhammad; Fahad, Shah; Wahid, Fazli; Arif, Muhammad; , Amanullah Journal: Journal of plant nutrition Issue: Volume 44:Number 11(2021) Page Start: 1598 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Intragenic deletion mutation in the gene desmoglein 4 underlies autosomal recessive hypotrichosis in six consanguineous families. Issue 3 (June 2016) Authors: Muhammad, Dost; Khan, Bushra; Raza, Syed I.; Ahmad, Farooq; Channa, Naseem A.; Ansar, Muhammad; Ahmad, Wasim; Basit, Sulman Journal: Journal of Taibah University medical sciences Issue: Volume 11:Issue 3(2016:Sep.) Page Start: 203 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutations in the lipase‐H gene causing autosomal recessive hypotrichosis and woolly hair. (13th March 2014) Authors: Mehmood, Sabba; Jan, Abid; Muhammad, Dost; Ahmad, Farooq; Mir, Hina; Younus, Muhammad; Ali, Ghazanfar; Ayub, Muhammad; Ansar, Muhammad; Ahmad, Wasim Journal: Australasian journal of dermatology Issue: Volume 56:Number 3(2015:Aug.) Page Start: e66 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Novel mutations in the genes TGM1 and ALOXE3 underlying autosomal recessive congenital ichthyosis. (17th November 2015) Authors: Ullah, Rahim; Ansar, Muhammad; Durrani, Zaka Ullah; Lee, Kwanghyuk; Santos‐Cortez, Regie Lyn P.; Muhammad, Dost; Ali, Mahboob; Zia, Muhammad; Ayub, Muhammad; Khan, Suliman; Smith, Josh D.; Nickerson, Deborah A.; Shendure, Jay; Bamshad, Michael; Leal, Suzanne M.; Ahmad, Wasim Journal: International journal of dermatology Issue: Volume 55:Number 5(2016) Page Start: 524 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗