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Muhammad Ansar

Showing results (91-100 of 191) with videos related to

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Human Heredity|December 8, 2004
DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22Muhammad Ansar, Maria H Chahrour, Mohammad Amin Ud Din, et al.
Ophthalmic Genetics|August 10, 2022
A new nonsense mutation in <i>HMX1</i> in two siblings with oculoauricular syndromeMuhammad Ansar, Samra Javed, Hafiz Muhammad Azhar Baig, et al.
Virology Journal|June 24, 2011
NS4A protein as a marker of HCV history suggests that different HCV genotypes originally evolved from genotype 1bMuhammad T Sarwar, Humera Kausar, Bushra Ijaz, et al.
Genes|March 29, 2023
Live Birth of a Healthy Child in a Couple with Identical mtDNA Carrying a Pathogenic c.471_477delTTTAAAAinsG Variant in the <i>MOCS2</i> GeneMaria Tofilo, Natalia Voronova, Leila Nigmatullina, et al.
Klinische Padiatrie|September 20, 2021
Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous FamiliesWarda Nawal, Asmat Ullah, Ubaid Ullah, et al.
Frontiers in Plant Science|September 20, 2023
Characterizing indigenous plant growth promoting bacteria and their synergistic effects with organic and chemical fertilizers on wheat (<i>Triticum aestivum</i>)Israr Asghar, Maqsood Ahmed, Muhammad Ansar Farooq, et al.
Genes|May 27, 2026
Expanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani FamiliesRazia Parveen, Muhammad Iqbal, Shahbaz Khan, et al.
Journal of Human Genetics|September 23, 2011
A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13Muhammad Ansar, Kwanghyuk Lee, Syed Kamran-Ul-Hassan Naqvi, et al.
American Journal of Medical Genetics. Part A|January 11, 2005
A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3Muhammad Aslam, Muhammad Wajid, Maria H Chahrour, et al.
Human Heredity|July 8, 2011
Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3Ghazanfar Ali, Kwanghyuk Lee, Paula B Andrade, et al.
Pageof 20

Showing results (91-100 of 191) with videos related to

Sort By:
Pageof 20
Human Heredity|December 8, 2004
DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22Muhammad Ansar, Maria H Chahrour, Mohammad Amin Ud Din, et al.
Ophthalmic Genetics|August 10, 2022
A new nonsense mutation in <i>HMX1</i> in two siblings with oculoauricular syndromeMuhammad Ansar, Samra Javed, Hafiz Muhammad Azhar Baig, et al.
Virology Journal|June 24, 2011
NS4A protein as a marker of HCV history suggests that different HCV genotypes originally evolved from genotype 1bMuhammad T Sarwar, Humera Kausar, Bushra Ijaz, et al.
Genes|March 29, 2023
Live Birth of a Healthy Child in a Couple with Identical mtDNA Carrying a Pathogenic c.471_477delTTTAAAAinsG Variant in the <i>MOCS2</i> GeneMaria Tofilo, Natalia Voronova, Leila Nigmatullina, et al.
Klinische Padiatrie|September 20, 2021
Loss of Function Variants in the XPC Causes Severe Xeroderma Pigmentosum in Three Large Consanguineous FamiliesWarda Nawal, Asmat Ullah, Ubaid Ullah, et al.
Frontiers in Plant Science|September 20, 2023
Characterizing indigenous plant growth promoting bacteria and their synergistic effects with organic and chemical fertilizers on wheat (<i>Triticum aestivum</i>)Israr Asghar, Maqsood Ahmed, Muhammad Ansar Farooq, et al.
Genes|May 27, 2026
Expanding the Genetic Landscape of Congenital Stationary Night Blindness Through the Analysis of Consanguineous Pakistani FamiliesRazia Parveen, Muhammad Iqbal, Shahbaz Khan, et al.
Journal of Human Genetics|September 23, 2011
A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13Muhammad Ansar, Kwanghyuk Lee, Syed Kamran-Ul-Hassan Naqvi, et al.
American Journal of Medical Genetics. Part A|January 11, 2005
A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3Muhammad Aslam, Muhammad Wajid, Maria H Chahrour, et al.
Human Heredity|July 8, 2011
Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3Ghazanfar Ali, Kwanghyuk Lee, Paula B Andrade, et al.
Pageof 20