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S Riazuddin

Showing results (31-40 of 60) with videos related to

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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.
Hemoglobin|March 18, 2000
Hb Sallanches [alpha104(G11)Cys-->Tyr]: a rare alpha2-globin chain variant found in the homozygous state in three members of a Pakistani familyS N Khan, F I Butt, S Riazuddin, et al.
Journal of Medical Genetics|August 3, 2004
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionS Naz, A J Griffith, S Riazuddin, et al.
Clinical Genetics|August 5, 2009
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15A M Waryah, A Rehman, Z M Ahmed, et al.
American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.
Nucleic Acids Research|August 25, 1987
DNA glycosylase enzymes induced during chemical adaptation of M. luteusS Riazuddin, A Athar, Z Ahmed, 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.
Osteoarthritis and Cartilage|August 17, 2014
Combination of ADMSCs and chondrocytes reduces hypertrophy and improves the functional properties of osteoarthritic cartilageM R Ahmed, A Mehmood, F-ur-R Bhatti, et al.
Current Opinion in Neurobiology|September 12, 2000
Modifier genes of hereditary hearing lossT Friedman, J Battey, B Kachar, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
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.
Hemoglobin|March 18, 2000
Hb Sallanches [alpha104(G11)Cys-->Tyr]: a rare alpha2-globin chain variant found in the homozygous state in three members of a Pakistani familyS N Khan, F I Butt, S Riazuddin, et al.
Journal of Medical Genetics|August 3, 2004
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunctionS Naz, A J Griffith, S Riazuddin, et al.
Clinical Genetics|August 5, 2009
DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15A M Waryah, A Rehman, Z M Ahmed, et al.
American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.
Nucleic Acids Research|August 25, 1987
DNA glycosylase enzymes induced during chemical adaptation of M. luteusS Riazuddin, A Athar, Z Ahmed, 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.
Osteoarthritis and Cartilage|August 17, 2014
Combination of ADMSCs and chondrocytes reduces hypertrophy and improves the functional properties of osteoarthritic cartilageM R Ahmed, A Mehmood, F-ur-R Bhatti, et al.
Current Opinion in Neurobiology|September 12, 2000
Modifier genes of hereditary hearing lossT Friedman, J Battey, B Kachar, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Pageof 6