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Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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P N Ray

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Journal of Medical Genetics|December 1, 1986

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyM W Thompson, P N Ray, B Belfall, et al.

American Journal of Human Genetics|May 1, 1992

Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibersC J Klein, D D Coovert, D E Bulman, et al.

Journal of Medical Genetics|December 1, 1986

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.

Journal of Medical Genetics|June 1, 1988

Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.

Science (New York, N.Y.)|September 25, 1987

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophyS E Bodrug, P N Ray, I L Gonzalez, et al.

Journal of Medical Genetics|July 1, 1990

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophyS E Bodrug, J R Roberson, L Weiss, et al.

Investigative Ophthalmology & Visual Science|February 1, 1995

mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophyD A Pillers, R G Weleber, W R Woodward, et al.

American Journal of Human Genetics|August 1, 1991

Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girlJ T Clarke, W L Greer, P M Strasberg, et al.

Diseases of the Colon and Rectum|February 1, 1994

Combined use of molecular and biomarkers for presymptomatic carrier risk assessment in familial adenomatous polyposis: implications for screening guidelinesB V Bapat, J A Parker, T Berk, et al.

Human Molecular Genetics|August 13, 1998

Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retinaP L Howard, G Y Dally, M H Wong, et al.

Pageof 11

Search research articles

Showing results (71-80 of 110) with videos related to

Sort By:

Pageof 11

Journal of Medical Genetics|December 1, 1986

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophyM W Thompson, P N Ray, B Belfall, et al.

American Journal of Human Genetics|May 1, 1992

Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibersC J Klein, D D Coovert, D E Bulman, et al.

Journal of Medical Genetics|December 1, 1986

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophyV M Kean, H L Macleod, M W Thompson, et al.

Journal of Medical Genetics|June 1, 1988

Partial gene duplication in Duchenne and Becker muscular dystrophiesX Y Hu, A H Burghes, P N Ray, et al.

Science (New York, N.Y.)|September 25, 1987

Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophyS E Bodrug, P N Ray, I L Gonzalez, et al.

Journal of Medical Genetics|July 1, 1990

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophyS E Bodrug, J R Roberson, L Weiss, et al.

Investigative Ophthalmology & Visual Science|February 1, 1995

mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophyD A Pillers, R G Weleber, W R Woodward, et al.

American Journal of Human Genetics|August 1, 1991

Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girlJ T Clarke, W L Greer, P M Strasberg, et al.

Diseases of the Colon and Rectum|February 1, 1994

Combined use of molecular and biomarkers for presymptomatic carrier risk assessment in familial adenomatous polyposis: implications for screening guidelinesB V Bapat, J A Parker, T Berk, et al.

Human Molecular Genetics|August 13, 1998

Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retinaP L Howard, G Y Dally, M H Wong, et al.

Pageof 11