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G A Nicholson

Showing results (71-80 of 115) with videos related to

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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.
The British Journal of Surgery|August 14, 2013
Contribution of surgical specialization to improved colorectal cancer survivalR Oliphant, G A Nicholson, P G Horgan, et al.
Neurology|February 2, 2011
A retrospective review of X-linked Charcot-Marie-Tooth disease in childhoodE M Yiu, N Geevasinga, G A Nicholson, et al.
Human Heredity|January 1, 1989
The B subunit of coagulation factor XIII is linked to renin and the Duffy blood group to alpha-spectrin on human chromosome 1L R Griffiths, P G Board, M B Zwi, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindredK L Williams, J C Durnall, A D Thoeng, et al.
Human Molecular Genetics|April 18, 1998
Evidence for an X-linked genetic component in familial typical migraineD R Nyholt, J L Dawkins, P J Brimage, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|June 4, 2015
Laparoscopic rectopexy is feasible and safe in the emergency admission settingA L A Bloemendaal, A Mishra, G A Nicholson, 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.
Pageof 12

Showing results (71-80 of 115) with videos related to

Sort By:
Pageof 12
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.
The British Journal of Surgery|August 14, 2013
Contribution of surgical specialization to improved colorectal cancer survivalR Oliphant, G A Nicholson, P G Horgan, et al.
Neurology|February 2, 2011
A retrospective review of X-linked Charcot-Marie-Tooth disease in childhoodE M Yiu, N Geevasinga, G A Nicholson, et al.
Human Heredity|January 1, 1989
The B subunit of coagulation factor XIII is linked to renin and the Duffy blood group to alpha-spectrin on human chromosome 1L R Griffiths, P G Board, M B Zwi, 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.
Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
A novel TARDBP mutation in an Australian amyotrophic lateral sclerosis kindredK L Williams, J C Durnall, A D Thoeng, et al.
Human Molecular Genetics|April 18, 1998
Evidence for an X-linked genetic component in familial typical migraineD R Nyholt, J L Dawkins, P J Brimage, et al.
Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland|June 4, 2015
Laparoscopic rectopexy is feasible and safe in the emergency admission settingA L A Bloemendaal, A Mishra, G A Nicholson, 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.
Pageof 12