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T B Friedman

Showing results (21-30 of 86) with videos related to

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Journal of Muscle Research and Cell Motility|April 20, 2002
Human myosin XVBP is a transcribed pseudogeneE T Boger, J R Sellers, T B Friedman
Oral Diseases|June 5, 2016
Unresolved questions regarding human hereditary deafnessA U Rehman, T B Friedman, A J Griffith
Clinical Genetics|January 26, 2007
A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1S Kitajiri, T Makishima, T B Friedman, et al.
Human Mutation|January 1, 1996
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndromeJ H Asher, A Sommer, R Morell, et al.
Journal of Medical Genetics|June 1, 1997
The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1)R Morell, T B Friedman, J H Asher, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1985
On the loss of uricolytic activity during primate evolution--I. Silencing of urate oxidase in a hominoid ancestorT B Friedman, G E Polanco, J C Appold, et al.
Journal of Medical Genetics|April 16, 1998
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7M L Carey, T B Friedman, J H Asher, et al.
Human Molecular Genetics|July 11, 1992
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian familyR Morell, T B Friedman, S Moeljopawiro, et al.
Gene|January 1, 1987
Cloning of a Drosophila melanogaster adenine phosphoribosyltransferase structural gene and deduced amino acid sequence of the enzymeD H Johnson, J E Edström, J B Burnett, et al.
Gene|October 16, 1999
PAX3 gene structure, alternative splicing and evolutionT D Barber, M C Barber, T E Cloutier, et al.
Pageof 9

Showing results (21-30 of 86) with videos related to

Sort By:
Pageof 9
Journal of Muscle Research and Cell Motility|April 20, 2002
Human myosin XVBP is a transcribed pseudogeneE T Boger, J R Sellers, T B Friedman
Oral Diseases|June 5, 2016
Unresolved questions regarding human hereditary deafnessA U Rehman, T B Friedman, A J Griffith
Clinical Genetics|January 26, 2007
A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1S Kitajiri, T Makishima, T B Friedman, et al.
Human Mutation|January 1, 1996
Missense mutation in the paired domain of PAX3 causes craniofacial-deafness-hand syndromeJ H Asher, A Sommer, R Morell, et al.
Journal of Medical Genetics|June 1, 1997
The incidence of deafness is non-randomly distributed among families segregating for Waardenburg syndrome type 1 (WS1)R Morell, T B Friedman, J H Asher, et al.
Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1985
On the loss of uricolytic activity during primate evolution--I. Silencing of urate oxidase in a hominoid ancestorT B Friedman, G E Polanco, J C Appold, et al.
Journal of Medical Genetics|April 16, 1998
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7M L Carey, T B Friedman, J H Asher, et al.
Human Molecular Genetics|July 11, 1992
A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian familyR Morell, T B Friedman, S Moeljopawiro, et al.
Gene|January 1, 1987
Cloning of a Drosophila melanogaster adenine phosphoribosyltransferase structural gene and deduced amino acid sequence of the enzymeD H Johnson, J E Edström, J B Burnett, et al.
Gene|October 16, 1999
PAX3 gene structure, alternative splicing and evolutionT D Barber, M C Barber, T E Cloutier, et al.
Pageof 9