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C Dodé

Showing results (21-30 of 35) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.
Genomics|September 1, 1995
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)P Guilford, C Dodé, F Crozet, et al.
Neuropediatrics|February 1, 1996
Neurosensory hearing loss in secondary adhalinopathyK Oexle, R Herrmann, C Dodé, et al.
American Journal of Hematology|July 1, 1988
Hemoglobin J Guantanamo [alpha 2 beta 2 128 (H6) Ala----Asp] in association with hemoglobin C and alpha-thalassemia in a family from BeninH Wajcman, V Baudin-Chich, J Kister, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.
Dermatology (Basel, Switzerland)|April 4, 2003
CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromesB Granel, N Philip, J Serratrice, et al.
Arthritis and Rheumatism|July 21, 2000
A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French familyC Dodé, T Papo, C Fieschi, et al.
Human Molecular Genetics|August 1, 1996
Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elementsJ Flint, J Rochette, C F Craddock, et al.
Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.
American Journal of Human Genetics|June 12, 1999
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implicationsC Cazeneuve, T Sarkisian, C Pêcheux, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Journal of Neurology, Neurosurgery, and Psychiatry|March 7, 1998
Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriersV Hahn-Barma, B Deweer, A Dürr, et al.
Genomics|September 1, 1995
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)P Guilford, C Dodé, F Crozet, et al.
Neuropediatrics|February 1, 1996
Neurosensory hearing loss in secondary adhalinopathyK Oexle, R Herrmann, C Dodé, et al.
American Journal of Hematology|July 1, 1988
Hemoglobin J Guantanamo [alpha 2 beta 2 128 (H6) Ala----Asp] in association with hemoglobin C and alpha-thalassemia in a family from BeninH Wajcman, V Baudin-Chich, J Kister, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.
Dermatology (Basel, Switzerland)|April 4, 2003
CIAS1 mutation in a patient with overlap between Muckle-Wells and chronic infantile neurological cutaneous and articular syndromesB Granel, N Philip, J Serratrice, et al.
Arthritis and Rheumatism|July 21, 2000
A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French familyC Dodé, T Papo, C Fieschi, et al.
Human Molecular Genetics|August 1, 1996
Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elementsJ Flint, J Rochette, C F Craddock, et al.
Neurology|March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patientsG Stevanin, A Camuzat, S E Holmes, et al.
American Journal of Human Genetics|June 12, 1999
MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implicationsC Cazeneuve, T Sarkisian, C Pêcheux, et al.
Pageof 4