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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

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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

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H Kokotas

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Clinical Genetics|February 6, 2010

Clinical and molecular aspects of aniridiaH Kokotas, M B Petersen

Clinical Genetics|May 11, 2007

Mitochondrial deafnessH Kokotas, M B Petersen, P J Willems

Clinical Genetics|March 23, 2011

High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosisS Orrù, E Manolakos, N Orrù, et al.

Cytogenetic and Genome Research|September 7, 2006

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual faceC Sarri, Y Gyftodimou, M Grigoriadou, et al.

Pageof 1

Search research articles

Showing results (1-10 of 4) with videos related to

Sort By:

Pageof 1

Clinical Genetics|February 6, 2010

Clinical and molecular aspects of aniridiaH Kokotas, M B Petersen

Clinical Genetics|May 11, 2007

Mitochondrial deafnessH Kokotas, M B Petersen, P J Willems

Clinical Genetics|March 23, 2011

High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosisS Orrù, E Manolakos, N Orrù, et al.

Cytogenetic and Genome Research|September 7, 2006

Supernumerary marker chromosome 5 diagnosed by M-FISH in a child with congenital heart defect and unusual faceC Sarri, Y Gyftodimou, M Grigoriadou, et al.

Pageof 1