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S Bundey

Showing results (91-100 of 99) with videos related to

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American Journal of Human Genetics|October 1, 1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneityD A Collier, T G Barrett, D Curtis, et al.
Nature Genetics|October 1, 1993
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathyZ Y Chen, E M Battinelli, A Fielder, et al.
Human Molecular Genetics|June 1, 1997
A novel mechanism of aberrant pre-mRNA splicing in humansJ D Cogan, M A Prince, S Lekhakula, et al.
American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.
American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.
American Journal of Human Genetics|March 26, 1999
A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variationX Z Liu, C Hope, C Y Liang, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndromeX Z Liu, C Hope, J Walsh, et al.
Pageof 10

Showing results (91-100 of 99) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 99 results.
American Journal of Human Genetics|October 1, 1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneityD A Collier, T G Barrett, D Curtis, et al.
Nature Genetics|October 1, 1993
A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathyZ Y Chen, E M Battinelli, A Fielder, et al.
Human Molecular Genetics|June 1, 1997
A novel mechanism of aberrant pre-mRNA splicing in humansJ D Cogan, M A Prince, S Lekhakula, et al.
American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
Journal of Medical Genetics|November 1, 1994
Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 lociM A Aldred, P W Teague, M Jay, et al.
American Journal of Human Genetics|February 11, 1999
A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25D P McHale, S Mitchell, S Bundey, et al.
American Journal of Human Genetics|March 26, 1999
A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variationX Z Liu, C Hope, C Y Liang, et al.
American Journal of Human Genetics|August 27, 1998
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndromeX Z Liu, C Hope, J Walsh, et al.
Pageof 10