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M L Kennerson

Showing results (1-10 of 17) with videos related to

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Genomics|October 27, 1998
Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeatM L Kennerson, N T Nassif, G A Nicholson
Clinical Chemistry|August 1, 1995
Detection of Charcot-Marie-Tooth type 1A duplication by the polymerase chain reactionI P Blair, M L Kennerson, G A Nicholson
Genetic Testing|July 30, 2003
A rapid and definitive test for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies using multiplexed real-time PCRP Lorentzos, T Kaiser, M L Kennerson, et al.
Neurology|December 13, 2006
Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth diseaseI G Huttner, M L Kennerson, S W Reddel, et al.
Clinical Genetics|December 15, 2015
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathiesS Tey, A Ahmad-Annuar, A P Drew, et al.
American Journal of Human Genetics|July 19, 2003
A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24C Kok, M L Kennerson, P J Spring, et al.
Genomics|December 24, 1997
The Charcot-Marie-Tooth binary repeat contains a gene transcribed from the opposite strand of a partially duplicated region of the COX10 geneM L Kennerson, N T Nassif, J L Dawkins, et al.
American Journal of Human Genetics|September 5, 2001
Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2M L Kennerson, D Zhu, R J Gardner, et al.
American Journal of Medical Genetics|November 1, 1992
Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplicationG A Nicholson, M L Kennerson, B J Keats, et al.
Archives of Neurology|November 1, 1994
Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20S F Berkovic, M L Kennerson, R A Howell, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Genomics|October 27, 1998
Genomic structure and physical mapping of C17orf1: a gene associated with the proximal element of the CMT1A-REP binary repeatM L Kennerson, N T Nassif, G A Nicholson
Clinical Chemistry|August 1, 1995
Detection of Charcot-Marie-Tooth type 1A duplication by the polymerase chain reactionI P Blair, M L Kennerson, G A Nicholson
Genetic Testing|July 30, 2003
A rapid and definitive test for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies using multiplexed real-time PCRP Lorentzos, T Kaiser, M L Kennerson, et al.
Neurology|December 13, 2006
Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth diseaseI G Huttner, M L Kennerson, S W Reddel, et al.
Clinical Genetics|December 15, 2015
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathiesS Tey, A Ahmad-Annuar, A P Drew, et al.
American Journal of Human Genetics|July 19, 2003
A locus for hereditary sensory neuropathy with cough and gastroesophageal reflux on chromosome 3p22-p24C Kok, M L Kennerson, P J Spring, et al.
Genomics|December 24, 1997
The Charcot-Marie-Tooth binary repeat contains a gene transcribed from the opposite strand of a partially duplicated region of the COX10 geneM L Kennerson, N T Nassif, J L Dawkins, et al.
American Journal of Human Genetics|September 5, 2001
Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2M L Kennerson, D Zhu, R J Gardner, et al.
American Journal of Medical Genetics|November 1, 1992
Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplicationG A Nicholson, M L Kennerson, B J Keats, et al.
Archives of Neurology|November 1, 1994
Phenotypic expression of benign familial neonatal convulsions linked to chromosome 20S F Berkovic, M L Kennerson, R A Howell, et al.
Pageof 2