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Saima Riazuddin

Showing results (51-60 of 135) with videos related to

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Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Investigative Ophthalmology & Visual Science|December 23, 2011
GNAT1 associated with autosomal recessive congenital stationary night blindnessMuhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, et al.
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Plos One|October 2, 2015
A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic FamilyKunjan Patel, Arnaud P Giese, J M Grossheim, et al.
Genes|April 3, 2021
Genetic Causes of Oculocutaneous Albinism in Pakistani PopulationZureesha Sajid, Sairah Yousaf, Yar M Waryah, et al.
Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.
Pageof 14

Showing results (51-60 of 135) with videos related to

Sort By:
Pageof 14
Journal of Human Genetics|June 3, 2011
Molecular and clinical studies of X-linked deafness among Pakistani familiesAli M Waryah, Zubair M Ahmed, Munir A Bhinder, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
Human Genetics|July 11, 2002
Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHICZubair M Ahmed, Tenesha N Smith, Saima Riazuddin, et al.
Ear and Hearing|August 19, 2003
Recent advances in the understanding of syndromic forms of hearing lossThomas B Friedman, Julie M Schultz, Tamar Ben-Yosef, et al.
Investigative Ophthalmology & Visual Science|December 23, 2011
GNAT1 associated with autosomal recessive congenital stationary night blindnessMuhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, et al.
Human Molecular Genetics|October 23, 2003
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23Zubair M Ahmed, Saima Riazuddin, Jamil Ahmad, et al.
Human Genetics|August 11, 2007
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3Quratul Ain, Sabiha Nazli, Saima Riazuddin, et al.
Plos One|October 2, 2015
A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic FamilyKunjan Patel, Arnaud P Giese, J M Grossheim, et al.
Genes|April 3, 2021
Genetic Causes of Oculocutaneous Albinism in Pakistani PopulationZureesha Sajid, Sairah Yousaf, Yar M Waryah, et al.
Human Genetics|June 21, 2020
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing lossKevin T Booth, Amama Ghaffar, Muhammad Rashid, et al.
Pageof 14