P F Chance - JoVE Visualize

Search research articles

ABOUT JoVE

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

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

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

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

P F Chance

Showing results (51-60 of 78) with videos related to

Pageof 8

Sort By:

Human Mutation|January 1, 1996

Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth diseaseB B Roa, L E Warner, C A Garcia, et al.

Human Mutation|January 1, 1997

Facilitated diagnosis of CMT1A duplication in chromosome 17p11.2-12: analysis with a CMT1A-REP repeat probe and photostimulated luminescence imagingT Ikegami, H Ikeda, P F Chance, et al.

Neurogenetics|November 11, 2006

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndromeA G Bassuk, Y Z Chen, S D Batish, et al.

Human Molecular Genetics|February 1, 1994

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17P F Chance, N Abbas, M W Lensch, et al.

American Journal of Human Genetics|March 21, 2000

X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3C L Bennett, R Yoshioka, H Kiyosawa, et al.

American Journal of Human Genetics|January 1, 1992

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markersR V Lebo, E D Lynch, T D Bird, et al.

Neurology|August 1, 1997

Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III)D R Lynch, H Hara, S W Yum, et al.

Nature Genetics|March 1, 1995

A 2D crossover-based map of the human X chromosome as a model for map integrationP R Fain, E N Kort, P F Chance, et al.

Annals of Neurology|May 1, 1994

Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresisP J Dyck, W J Litchy, S Minnerath, et al.

American Journal of Human Genetics|April 29, 1998

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34P F Chance, B A Rabin, S G Ryan, et al.

Pageof 8

Search research articles

Showing results (51-60 of 78) with videos related to

Sort By:

Pageof 8

Human Mutation|January 1, 1996

Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth diseaseB B Roa, L E Warner, C A Garcia, et al.

Human Mutation|January 1, 1997

Facilitated diagnosis of CMT1A duplication in chromosome 17p11.2-12: analysis with a CMT1A-REP repeat probe and photostimulated luminescence imagingT Ikegami, H Ikeda, P F Chance, et al.

Neurogenetics|November 11, 2006

In cis autosomal dominant mutation of Senataxin associated with tremor/ataxia syndromeA G Bassuk, Y Z Chen, S D Batish, et al.

Human Molecular Genetics|February 1, 1994

Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17P F Chance, N Abbas, M W Lensch, et al.

American Journal of Human Genetics|March 21, 2000

X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3C L Bennett, R Yoshioka, H Kiyosawa, et al.

American Journal of Human Genetics|January 1, 1992

Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markersR V Lebo, E D Lynch, T D Bird, et al.

Neurology|August 1, 1997

Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III)D R Lynch, H Hara, S W Yum, et al.

Nature Genetics|March 1, 1995

A 2D crossover-based map of the human X chromosome as a model for map integrationP R Fain, E N Kort, P F Chance, et al.

Annals of Neurology|May 1, 1994

Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresisP J Dyck, W J Litchy, S Minnerath, et al.

American Journal of Human Genetics|April 29, 1998

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34P F Chance, B A Rabin, S G Ryan, et al.

Pageof 8