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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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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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Robert P Erickson

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American Journal of Human Genetics|June 28, 2011

Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial cleftingIrfan Saadi, Fowzan S Alkuraya, Stephen S Gisselbrecht, et al.

Human Molecular Genetics|November 4, 2011

A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutationsRobert A Maue, Robert W Burgess, Bing Wang, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome regionJonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.

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Search research articles

Showing results (111-120 of 113) with videos related to

Sort By:

Pageof 12

You have reached the last page of results.This site can display upto 113 results.

American Journal of Human Genetics|June 28, 2011

Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial cleftingIrfan Saadi, Fowzan S Alkuraya, Stephen S Gisselbrecht, et al.

Human Molecular Genetics|November 4, 2011

A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutationsRobert A Maue, Robert W Burgess, Bing Wang, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 2, 2007

Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome regionJonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.

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