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Z M Ahmed

Showing results (1-10 of 20) with videos related to

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Radiography|July 1, 1988
Impedence phlebographyZ M Ahmed
Clinical Genetics|June 6, 2003
The molecular genetics of Usher syndromeZ M Ahmed, S Riazuddin, S Riazuddin, et al.
Clinical Genetics|October 12, 2012
OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24T Kausar, M A Bhatti, M Ali, et al.
Clinical Genetics|September 24, 2017
INPP5K variant causes autosomal recessive congenital cataract in a Pakistani familyS Yousaf, S A Sheikh, S Riazuddin, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
An Open-Source Tool for Automated Human-Level Circling Behavior DetectionO R Stanley, A Swaminathan, E Wojahn, et al.
Scientific Reports|September 8, 2024
An open-source tool for automated human-level circling behavior detectionO R Stanley, A Swaminathan, E Wojahn, et al.
Clinical Genetics|May 29, 2008
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23Z M Ahmed, S Riazuddin, S N Khan, et al.
Journal of Medical Genetics|April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)S A Mohiddin, Z M Ahmed, A J Griffith, et al.
Clinical Genetics|January 4, 2012
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3R A Ali, A U Rehman, S N Khan, et al.
Clinical Genetics|March 3, 2009
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in PakistanB Y Choi, Z M Ahmed, S Riazuddin, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Radiography|July 1, 1988
Impedence phlebographyZ M Ahmed
Clinical Genetics|June 6, 2003
The molecular genetics of Usher syndromeZ M Ahmed, S Riazuddin, S Riazuddin, et al.
Clinical Genetics|October 12, 2012
OCA5, a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24T Kausar, M A Bhatti, M Ali, et al.
Clinical Genetics|September 24, 2017
INPP5K variant causes autosomal recessive congenital cataract in a Pakistani familyS Yousaf, S A Sheikh, S Riazuddin, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
An Open-Source Tool for Automated Human-Level Circling Behavior DetectionO R Stanley, A Swaminathan, E Wojahn, et al.
Scientific Reports|September 8, 2024
An open-source tool for automated human-level circling behavior detectionO R Stanley, A Swaminathan, E Wojahn, et al.
Clinical Genetics|May 29, 2008
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23Z M Ahmed, S Riazuddin, S N Khan, et al.
Journal of Medical Genetics|April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)S A Mohiddin, Z M Ahmed, A J Griffith, et al.
Clinical Genetics|January 4, 2012
DFNB86, a novel autosomal recessive non-syndromic deafness locus on chromosome 16p13.3R A Ali, A U Rehman, S N Khan, et al.
Clinical Genetics|March 3, 2009
Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in PakistanB Y Choi, Z M Ahmed, S Riazuddin, et al.
Pageof 2