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W Ahmad

Showing results (91-100 of 193) with videos related to

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Iranian Journal of Public Health|November 21, 2015
Determinants of Mortality in First-Ever Stroke Patients in the Suburban Malaysia: A Retrospective Hospital-Based Study, 2005-2011Nadiah Wan-Arfah, W Ahmad Wan Muhamad Amir, Mustapha Muzaimi, et al.
The British Journal of Dermatology|September 18, 2008
A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)S Kamran-ul-Hassan Naqvi, S I Raza, A K Naveed, et al.
The British Journal of Dermatology|March 7, 2013
Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous familiesR H Ali, R Habib, N Ud-Din, et al.
Experimental Dermatology|May 8, 1999
Identification of a de novo glycine substitution in the type VII collagen gene in a proband with mild dystrophic epidermolysis bullosaP B Cserhalmi-Friedman, J Grossman, S Karpati, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|October 4, 2017
Predictors of poor treatment outcomes in multidrug-resistant tuberculosis patients: a retrospective cohort studyA Javaid, I Ullah, H Masud, et al.
Operative Dentistry|March 6, 2015
Cuspal Flexure and Extent of Cure of a Bulk-fill Flowable Base CompositeA V Francis, A D Braxton, W Ahmad, et al.
Clinical Genetics|May 23, 2006
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12S Malik, A A Abbasi, M Ansar, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|August 10, 2007
Aposthia: a birth defect or normal quantitative recessive human genetic trait?M Amin-Ud-Din, A Salam, M A Rafiq, et al.
Risk Management and Healthcare Policy|March 4, 2021
A Cross-Sectional Survey on Occupational Blood and Body Fluid Exposure Risk in a Tertiary Hospital in East MalaysiaChe Wan Ilmiyah C W Ahmad, Khamisah Awang Lukman, Raja Muhammad Raja Omar, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22W Ahmad, S Li, H Chen, et al.
Pageof 20

Showing results (91-100 of 193) with videos related to

Sort By:
Pageof 20
Iranian Journal of Public Health|November 21, 2015
Determinants of Mortality in First-Ever Stroke Patients in the Suburban Malaysia: A Retrospective Hospital-Based Study, 2005-2011Nadiah Wan-Arfah, W Ahmad Wan Muhamad Amir, Mustapha Muzaimi, et al.
The British Journal of Dermatology|September 18, 2008
A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2)S Kamran-ul-Hassan Naqvi, S I Raza, A K Naveed, et al.
The British Journal of Dermatology|March 7, 2013
Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous familiesR H Ali, R Habib, N Ud-Din, et al.
Experimental Dermatology|May 8, 1999
Identification of a de novo glycine substitution in the type VII collagen gene in a proband with mild dystrophic epidermolysis bullosaP B Cserhalmi-Friedman, J Grossman, S Karpati, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|October 4, 2017
Predictors of poor treatment outcomes in multidrug-resistant tuberculosis patients: a retrospective cohort studyA Javaid, I Ullah, H Masud, et al.
Operative Dentistry|March 6, 2015
Cuspal Flexure and Extent of Cure of a Bulk-fill Flowable Base CompositeA V Francis, A D Braxton, W Ahmad, et al.
Clinical Genetics|May 23, 2006
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12S Malik, A A Abbasi, M Ansar, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|August 10, 2007
Aposthia: a birth defect or normal quantitative recessive human genetic trait?M Amin-Ud-Din, A Salam, M A Rafiq, et al.
Risk Management and Healthcare Policy|March 4, 2021
A Cross-Sectional Survey on Occupational Blood and Body Fluid Exposure Risk in a Tertiary Hospital in East MalaysiaChe Wan Ilmiyah C W Ahmad, Khamisah Awang Lukman, Raja Muhammad Raja Omar, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Lysosomal chitobiase (CTB) and the G-protein gamma 5 subunit (GNG5) genes co-localize to human chromosome 1p22W Ahmad, S Li, H Chen, et al.
Pageof 20