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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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P F Chance

Showing results (71-80 of 78) with videos related to

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Human Genetics|February 1, 1997

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPPM Yamamoto, T Yasuda, K Hayasaka, et al.

Human Genetics|November 1, 1991

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.

Neurology|January 15, 2003

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1CV A Street, C L Bennett, J D Goldy, et al.

Neurology|May 23, 2008

Late-onset hereditary axonal neuropathiesC L Bennett, V H Lawson, K L Brickell, et al.

Journal of Medical Genetics|September 13, 2005

AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.

Neurology|May 20, 2009

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.

Journal of Medical Genetics|November 27, 2009

Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophyA M B Collie, M L Landsverk, E Ruzzo, et al.

Journal of Medical Genetics|July 4, 2009

Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)D Doherty, M A Parisi, L S Finn, et al.

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Search research articles

Showing results (71-80 of 78) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 78 results.

Human Genetics|February 1, 1997

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPPM Yamamoto, T Yasuda, K Hayasaka, et al.

Human Genetics|November 1, 1991

Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene regionR V Lebo, P F Chance, P J Dyck, et al.

Neurology|January 15, 2003

Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1CV A Street, C L Bennett, J D Goldy, et al.

Neurology|May 23, 2008

Late-onset hereditary axonal neuropathiesC L Bennett, V H Lawson, K L Brickell, et al.

Journal of Medical Genetics|September 13, 2005

AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.

Neurology|May 20, 2009

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophyM C Hannibal, E K Ruzzo, L R Miller, et al.

Journal of Medical Genetics|November 27, 2009

Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophyA M B Collie, M L Landsverk, E Ruzzo, et al.

Journal of Medical Genetics|July 4, 2009

Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)D Doherty, M A Parisi, L S Finn, et al.

Pageof 8