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P F Chance

Showing results (41-50 of 78) with videos related to

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Brain : a Journal of Neurology|August 4, 1999
Autosomal dominant juvenile amyotrophic lateral sclerosisB A Rabin, J W Griffin, B J Crain, et al.
Annals of Neurology|December 1, 1983
Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I)T D Bird, J Ott, E R Giblett, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disordersP F Chance, M W Lensch, H Lipe, et al.
Neurology|December 1, 1992
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Comparison of single-strand conformation polymorphism and heteroduplex analysis for detection of mutations in Charcot-Marie-Tooth type 1 disease and related peripheral neuropathiesE Nelis, L E Warner, E D Vriendt, et al.
American Journal of Human Genetics|February 1, 1993
Linkage localization of X-linked Charcot-Marie-Tooth diseaseJ Bergoffen, J Trofatter, M A Pericak-Vance, et al.
Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.
Cancer|April 1, 1996
Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1AW D Graf, P F Chance, M W Lensch, et al.
Human Genetics|January 1, 1983
Regional localization of the human factor IX gene by molecular hybridizationP F Chance, K A Dyer, K Kurachi, et al.
The Journal of Clinical Investigation|December 1, 1985
An intragenic deletion of the factor IX gene in a family with hemophilia BS H Chen, S Yoshitake, P F Chance, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
Brain : a Journal of Neurology|August 4, 1999
Autosomal dominant juvenile amyotrophic lateral sclerosisB A Rabin, J W Griffin, B J Crain, et al.
Annals of Neurology|December 1, 1983
Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I)T D Bird, J Ott, E R Giblett, et al.
Neurology|December 1, 1994
Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct genetic disordersP F Chance, M W Lensch, H Lipe, et al.
Neurology|December 1, 1992
Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1AP F Chance, T D Bird, N Matsunami, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Comparison of single-strand conformation polymorphism and heteroduplex analysis for detection of mutations in Charcot-Marie-Tooth type 1 disease and related peripheral neuropathiesE Nelis, L E Warner, E D Vriendt, et al.
American Journal of Human Genetics|February 1, 1993
Linkage localization of X-linked Charcot-Marie-Tooth diseaseJ Bergoffen, J Trofatter, M A Pericak-Vance, et al.
Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.
Cancer|April 1, 1996
Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1AW D Graf, P F Chance, M W Lensch, et al.
Human Genetics|January 1, 1983
Regional localization of the human factor IX gene by molecular hybridizationP F Chance, K A Dyer, K Kurachi, et al.
The Journal of Clinical Investigation|December 1, 1985
An intragenic deletion of the factor IX gene in a family with hemophilia BS H Chen, S Yoshitake, P F Chance, et al.
Pageof 8