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A Mohyuddin

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

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Human Molecular Genetics|January 1, 1996
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from PakistanA Veske, R Oehlmann, F Younus, et al.
Nucleic Acids Research|December 22, 1999
Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database informationQ Ayub, A Mohyuddin, R Qamar, et al.
Genetic Testing|May 4, 2000
P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patientsS Khaliq, A Hameed, T Khaliq, et al.
Journal of Medical Genetics|May 3, 2005
Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosaS Khaliq, A Abid, M Ismail, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3H S Scott, S E Antonarakis, L Mittaz, et al.
The Pharmacogenomics Journal|July 30, 2008
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 geneM-Y Lee, N Mukherjee, A J Pakstis, et al.
Journal of Medical Genetics|May 16, 2002
Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomasA Mohyuddin, W J Neary, A Wallace, et al.
American Journal of Human Genetics|January 3, 2001
Y-chromosome lineages trace diffusion of people and languages in southwestern AsiaL Quintana-Murci, C Krausz, T Zerjal, 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.
Human Molecular Genetics|January 1, 1996
Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from PakistanA Veske, R Oehlmann, F Younus, et al.
Nucleic Acids Research|December 22, 1999
Identification and characterisation of novel human Y-chromosomal microsatellites from sequence database informationQ Ayub, A Mohyuddin, R Qamar, et al.
Genetic Testing|May 4, 2000
P53 mutations, polymorphisms, and haplotypes in Pakistani ethnic groups and breast cancer patientsS Khaliq, A Hameed, T Khaliq, et al.
Journal of Medical Genetics|May 3, 2005
Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosaS Khaliq, A Abid, M Ismail, et al.
Advances in Oto-Rhino-Laryngology|June 27, 2000
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3H S Scott, S E Antonarakis, L Mittaz, et al.
The Pharmacogenomics Journal|July 30, 2008
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 geneM-Y Lee, N Mukherjee, A J Pakstis, et al.
Journal of Medical Genetics|May 16, 2002
Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomasA Mohyuddin, W J Neary, A Wallace, et al.
American Journal of Human Genetics|January 3, 2001
Y-chromosome lineages trace diffusion of people and languages in southwestern AsiaL Quintana-Murci, C Krausz, T Zerjal, et al.
Pageof 2