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Memoona Ramzan

Showing results (11-20 of 18) with videos related to

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JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Journal of Medical Genetics|March 19, 2026
<i>CDK4</i> and <i>CDK6</i> variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosisEsra Isik, Mohammad Faraz Zafeer, Guney Bademci, et al.
Human Genomics|November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority populationLéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
Advanced Genetics (Hoboken, N.J.)|December 30, 2024
Extreme Phenotypic Variability of <i>ACTG1</i>-Related Disorders in Hearing LossMaria T Bernardi, Memoona Ramzan, Laura Calderon, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
The Journal of Clinical Investigation|September 30, 2025
Carboxypeptidase D deficiency causes hearing loss amenable to treatmentMemoona Ramzan, Natalie Ortiz-Vega, Mohammad Faraz Zafeer, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
JCI Insight|June 18, 2026
Distal enhancer-insulator module of GDF6 is essential for cochlear formationMohammad Faraz Zafeer, Clemer Abad, Havva Ortabozkoyun, et al.
Journal of Medical Genetics|March 19, 2026
<i>CDK4</i> and <i>CDK6</i> variants in patients with primary microcephaly lead to cell cycle defects and mitochondria-induced apoptosisEsra Isik, Mohammad Faraz Zafeer, Guney Bademci, et al.
Human Genomics|November 23, 2023
Dispersed DNA variants underlie hearing loss in South Florida's minority populationLéShon Peart, Joanna Gonzalez, Dayna Morel Swols, et al.
Advanced Genetics (Hoboken, N.J.)|December 30, 2024
Extreme Phenotypic Variability of <i>ACTG1</i>-Related Disorders in Hearing LossMaria T Bernardi, Memoona Ramzan, Laura Calderon, et al.
Human Mutation|July 15, 2021
Variants of human CLDN9 cause mild to profound hearing lossMemoona Ramzan, Christophe Philippe, Inna A Belyantseva, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Scientific Reports|May 5, 2026
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from PakistanMemoona Ramzan, Hafiza Idrees, Hina Khan, et al.
The Journal of Clinical Investigation|September 30, 2025
Carboxypeptidase D deficiency causes hearing loss amenable to treatmentMemoona Ramzan, Natalie Ortiz-Vega, Mohammad Faraz Zafeer, et al.
Pageof 2