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T B Friedman

Showing results (51-60 of 86) with videos related to

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American Journal of Human Genetics|July 21, 2000
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9S Yasunaga, M Grati, S Chardenoux, et al.
Human Molecular Genetics|September 1, 1994
Dinucleotide repeat polymorphism at D14S542M L Carey, Y Liang, T D Barber, et al.
Vision Research|January 1, 1981
Donor age influences the growth of rabbit lens epithelial cells in vitroJ R Reddan, T B Friedman, M K Mostafapour, et al.
Human Molecular Genetics|January 1, 1995
Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese populationR Morell, Y Liang, J H Asher, 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.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Clinical Genetics|November 22, 2007
Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing lossV Labay, G Garrido, A C Madeo, et al.
Journal of Medical Genetics|May 15, 2003
Distinctive audiometric profile associated with DFNB21 alleles of TECTAS Naz, F Alasti, A Mowjoodi, et al.
Nature Genetics|January 1, 1995
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17T B Friedman, Y Liang, J L Weber, 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 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|July 21, 2000
OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9S Yasunaga, M Grati, S Chardenoux, et al.
Human Molecular Genetics|September 1, 1994
Dinucleotide repeat polymorphism at D14S542M L Carey, Y Liang, T D Barber, et al.
Vision Research|January 1, 1981
Donor age influences the growth of rabbit lens epithelial cells in vitroJ R Reddan, T B Friedman, M K Mostafapour, et al.
Human Molecular Genetics|January 1, 1995
Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese populationR Morell, Y Liang, J H Asher, 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.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Clinical Genetics|November 22, 2007
Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing lossV Labay, G Garrido, A C Madeo, et al.
Journal of Medical Genetics|May 15, 2003
Distinctive audiometric profile associated with DFNB21 alleles of TECTAS Naz, F Alasti, A Mowjoodi, et al.
Nature Genetics|January 1, 1995
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17T B Friedman, Y Liang, J L Weber, 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 9