Tariq Muhammad | Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University
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概要
- TARIQ Muhammadの詳細を見る
- 同名の論文著者
- Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam Universityの論文著者
関連著者
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Tariq Muhammad
Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University
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Ahmad Wasim
Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University
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Siddiqui Hamid
Institute of Chemistry, University of the Punjab
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Siddiqui Hamid
Institute Of Chemistry University Of The Punjab
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Munir Christy
Department Of Chemistry Forman Christian College University
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Tariq Muhammad
Department Of Chemistry University Of Sargodha
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AHMAD Wasim
Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University
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RASHEED Khalid
Department of Chemistry, Quaid-i-Azam University
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HUSSAIN Ishtiaq
Institute of Chemistry University of the Punjab
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Rasheed Khalid
Department Of Chemistry Quaid-i-azam University
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WASIF Naveed
Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University
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Wasif Naveed
Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University
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Jelani Musharraf
Department Of Biochemistry Faculty Of Biological Sciences Quaid-i-azam University
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JAN Iftikhar
Department of Pediatric Surgery, National Institute of Rehabilitation Medicine (NIRM)
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ULLAH Hazrat
Department of Pediatric Surgery, National Institute of Rehabilitation Medicine (NIRM)
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NAEEM Muhammad
Department of Biotechnology, Faculty of Biological Sciences, Quaid-i-Azam University
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Ullah Hazrat
Department Of Pediatric Surgery National Institute Of Rehabilitation Medicine (nirm)
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Jan Iftikhar
Department Of Pediatric Surgery National Institute Of Rehabilitation Medicine (nirm)
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Naeem Muhammad
Department Of Biotechnology Faculty Of Biological Sciences Quaid-i-azam University
著作論文
- Synthesis, Characterization and Hypoglycemic Activity of Zn(II), Cd(II) and Hg(II) Complexes with Glibenclamide
- A novel missense mutation in the EVC gene underlies Ellis-van Creveld syndrome in a Pakistani family
- Congenital cutis laxa syndrome maps to a novel locus on chromosome 9q13-q21.32