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Author/Creator Muhammad, Dost

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
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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) ↗