Y H Fu - 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

Y H Fu

Showing results (91-100 of 94) with videos related to

Pageof 10

Sort By:

You have reached the last page of results.This site can display upto 94 results.

Neurology|November 10, 2004

Correlating phenotype and genotype in the periodic paralysesT M Miller, M R Dias da Silva, H A Miller, et al.

Neurology|May 23, 2007

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.

Neuron|October 3, 2001

Polyglutamine-expanded ataxin-7 antagonizes CRX function and induces cone-rod dystrophy in a mouse model of SCA7A R La Spada, Y H Fu, B L Sopher, et al.

Cell|May 24, 2001

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, et al.

Pageof 10

Search research articles

Showing results (91-100 of 94) with videos related to

Sort By:

Pageof 10

You have reached the last page of results.This site can display upto 94 results.

Neurology|November 10, 2004

Correlating phenotype and genotype in the periodic paralysesT M Miller, M R Dias da Silva, H A Miller, et al.

Neurology|May 23, 2007

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesiaM K Bruno, H-Y Lee, G W J Auburger, et al.

Neuron|October 3, 2001

Polyglutamine-expanded ataxin-7 antagonizes CRX function and induces cone-rod dystrophy in a mouse model of SCA7A R La Spada, Y H Fu, B L Sopher, et al.

Cell|May 24, 2001

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, et al.

Pageof 10