Showing 1 - 16 results of 16 for search 'Sabika FIRASAT', query time: 7.15s
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Genetic characterization of gigantocotyle explanatum from buffaloes in northwestern pakistan by Sana ULLAH, Kiran AFSHAN, Muhammad ARSHAD, Sabika FIRASAT
Published 2019-11-01
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Comparative efficacy of synthetic acaricides against tick infestations in goats by Ayesha MALIK, Kiran AFSHAN, Abdul RAZZAQ, Zahida FATIMA, Munib HUSSAIN, Sabika FIRASAT
Published 2021-02-01
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Screening of high-risk deleterious missense variations in the CYP1B1 gene implicated in the pathogenesis of primary congenital glaucoma: A comprehensive in silico approach by Muhammad Shahid, Ahmad Azfaralariff, Muhammad Tufail, Nazeer Hussain Khan, Ahmed Abdulkareem Najm, Sabika Firasat, Muhammad Zubair, Shazrul Fazry, Douglas Law
Published 2022-11-01
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Correction: Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan. by Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
Published 2023-01-01
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Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan by Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
Published 2022-01-01
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Mutational analysis in sodium-borate cotransporter SLC4A11 in consanguineous families from Punjab, Pakistan. by Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
Published 2022-01-01
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Identifying the genetic causes of phenotypically diagnosed Pakistani mucopolysaccharidoses patients by whole genome sequencing by Rutaba Gul, Rutaba Gul, Sabika Firasat, Mikkel Schubert, Asmat Ullah, Elionora Peña, Anne C. B. Thuesen, Mulazim Hussain, Frederik F. Staeger, Anette P. Gjesing, Anders Albrechtsen, Torben Hansen
Published 2023-04-01
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Identification of genetic variants associated with a wide spectrum of phenotypes clinically diagnosed as Sanfilippo and Morquio syndromes using whole genome sequencing by Rutaba Gul, Rutaba Gul, Sabika Firasat, Mikkel Schubert, Asmat Ullah, Elionora Peña, Anne C. B. Thuesen, Annete P. Gjesing, Mulazim Hussain, Muhammad Tufail, Muhammad Saqib, Muhammad Saqib, Kiran Afshan, Torben Hansen
Published 2023-09-01
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