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Shagufta Khaliq

Showing results (1-10 of 51) with videos related to

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Human Mutation|October 19, 2022
HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic associationAiysha Abid, Ali Raza, Tahir Aziz, et al.
JPMA. the Journal of the Pakistan Medical Association|December 12, 2023
Molecular Characterization of Haemoglobin ESara Ejaz, Ghulam Mustafa, Shagufta Khaliq, et al.
Pakistan Journal of Medical Sciences|March 28, 2024
Clinical utility of CLL-IPI scoring system in Pakistani Chronic Lymphocytic Patients: A single center experienceAisha Hameed, Nadia Sajid, Muhammad Fayyaz, et al.
JPMA. the Journal of the Pakistan Medical Association|December 1, 2011
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotypeSayed Hajan Shah, Aiysha Abid, Saba Shahid, et al.
JPMA. the Journal of the Pakistan Medical Association|October 1, 2016
Serum vitamin D levels and gene polymorphisms (Fok1 and Apa1) in children with type I diabetes and healthy controlsMaimoona Nasreen, Khalid Pervaiz Lone, Saba Khaliq, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|April 2, 2011
Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani familyAiysha Abid, Naveed Akhtar, Shagufta Khaliq, et al.
JPMA. the Journal of the Pakistan Medical Association|December 20, 2020
Six-year experience of prenatal diagnosis for beta thalassemia in twin pregnancies and selective foetal reduction - A case seriesYasmeen Ehsan, Shabnam Bashir, Furqan Sabir, et al.
Investigative Ophthalmology & Visual Science|July 2, 2002
A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani familyShagufta Khaliq, Abdul Hameed, Muhammad Ismail, et al.
Journal of Human Genetics|August 10, 2006
Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genesMuhammad Ismail, Aiysha Abid, Khalid Anwar, et al.
Journal of Biochemistry and Molecular Biology|October 14, 2004
Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and essential hypertension in young Pakistani patientsMuhammad Ismail, Naveed Akhtar, Muhammad Nasir, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Human Mutation|October 19, 2022
HOGA1 gene pathogenic variants in primary hyperoxaluria type III: Spectrum of pathogenic sequence variants, and phenotypic associationAiysha Abid, Ali Raza, Tahir Aziz, et al.
JPMA. the Journal of the Pakistan Medical Association|December 12, 2023
Molecular Characterization of Haemoglobin ESara Ejaz, Ghulam Mustafa, Shagufta Khaliq, et al.
Pakistan Journal of Medical Sciences|March 28, 2024
Clinical utility of CLL-IPI scoring system in Pakistani Chronic Lymphocytic Patients: A single center experienceAisha Hameed, Nadia Sajid, Muhammad Fayyaz, et al.
JPMA. the Journal of the Pakistan Medical Association|December 1, 2011
Identification of LIPH gene mutation in a consanguineous family segregating the woolly hair/hypotrichosis phenotypeSayed Hajan Shah, Aiysha Abid, Saba Shahid, et al.
JPMA. the Journal of the Pakistan Medical Association|October 1, 2016
Serum vitamin D levels and gene polymorphisms (Fok1 and Apa1) in children with type I diabetes and healthy controlsMaimoona Nasreen, Khalid Pervaiz Lone, Saba Khaliq, et al.
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP|April 2, 2011
Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani familyAiysha Abid, Naveed Akhtar, Shagufta Khaliq, et al.
JPMA. the Journal of the Pakistan Medical Association|December 20, 2020
Six-year experience of prenatal diagnosis for beta thalassemia in twin pregnancies and selective foetal reduction - A case seriesYasmeen Ehsan, Shabnam Bashir, Furqan Sabir, et al.
Investigative Ophthalmology & Visual Science|July 2, 2002
A novel locus for autosomal dominant nuclear cataract mapped to chromosome 2p12 in a Pakistani familyShagufta Khaliq, Abdul Hameed, Muhammad Ismail, et al.
Journal of Human Genetics|August 10, 2006
Refinement of the locus for autosomal recessive cone-rod dystrophy (CORD8) linked to chromosome 1q23-q24 in a Pakistani family and exclusion of candidate genesMuhammad Ismail, Aiysha Abid, Khalid Anwar, et al.
Journal of Biochemistry and Molecular Biology|October 14, 2004
Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and essential hypertension in young Pakistani patientsMuhammad Ismail, Naveed Akhtar, Muhammad Nasir, et al.
Pageof 6