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Memoona Ramzan

Showing results (1-10 of 18) with videos related to

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Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
Scientific Reports|July 19, 2020
Spectrum of genetic variants in moderate to severe sporadic hearing loss in PakistanMemoona Ramzan, Rasheeda Bashir, Midhat Salman, et al.
Scientific Reports|October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing lossMemoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Journal of Virological Methods|July 3, 2015
A cornucopia of screening and diagnostic techniques for human papillomavirus associated cervical carcinomasMemoona Ramzan, Noor ul Ain, Sadaf Ilyas, et al.
Biochemical Genetics|January 9, 2026
Spectrum of DNA Variants Underlying Deafness in an Ecuadorian CohortAnghela Reinoso-Castillo, Memoona Ramzan, Andrea Carrera-Gonzalez, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
Research Square|July 1, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear MalformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Human Genetics|January 9, 2025
Human organoids for rapid validation of gene variants linked to cochlear malformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Gene|April 28, 2019
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing lossMemoona Ramzan, Hafiza Idrees, Ghulam Mujtaba, et al.
Scientific Reports|July 19, 2020
Spectrum of genetic variants in moderate to severe sporadic hearing loss in PakistanMemoona Ramzan, Rasheeda Bashir, Midhat Salman, et al.
Scientific Reports|October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing lossMemoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Journal of Virological Methods|July 3, 2015
A cornucopia of screening and diagnostic techniques for human papillomavirus associated cervical carcinomasMemoona Ramzan, Noor ul Ain, Sadaf Ilyas, et al.
Biochemical Genetics|January 9, 2026
Spectrum of DNA Variants Underlying Deafness in an Ecuadorian CohortAnghela Reinoso-Castillo, Memoona Ramzan, Andrea Carrera-Gonzalez, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
Research Square|July 1, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear MalformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Human Genetics|January 9, 2025
Human organoids for rapid validation of gene variants linked to cochlear malformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
Clinical Genetics|August 31, 2016
Genetic causes of moderate to severe hearing loss point to modifiersSadaf Naz, Ayesha Imtiaz, Ghulam Mujtaba, et al.
Pageof 2