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C Piussan

Showing results (101-110 of 112) with videos related to

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Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|January 1, 1986
[ Chronic juvenile arthritis. Double-blind study of efficacy and tolerance of D-penicillamine]A M Prieur, C Piussan, P Manigne, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.
Archives Francaises De Pediatrie|February 1, 1985
[Juvenile chronic arthritis. Double-blind study of the efficacy and tolerance of D-penicillamine]A M Prieur, C Piussan, P Manigne, et al.
American Journal of Human Genetics|June 1, 1996
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markersK A Goddard, C E Yu, J Oshima, et al.
Annales De Pediatrie|January 1, 1990
[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]S Szpiro-Tapia, J Kaplan, A Pelet, et al.
Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Genomics|October 1, 1994
Homozygosity mapping of the Werner syndrome locus (WRN)J Nakura, E M Wijsman, T Miki, et al.
American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.
American Journal of Medical Genetics|March 9, 1999
Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenariansE Castro, C E Ogburn, K E Hunt, et al.
Pageof 12

Showing results (101-110 of 112) with videos related to

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Pageof 12
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|January 1, 1986
[ Chronic juvenile arthritis. Double-blind study of efficacy and tolerance of D-penicillamine]A M Prieur, C Piussan, P Manigne, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.
Archives Francaises De Pediatrie|February 1, 1985
[Juvenile chronic arthritis. Double-blind study of the efficacy and tolerance of D-penicillamine]A M Prieur, C Piussan, P Manigne, et al.
American Journal of Human Genetics|June 1, 1996
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markersK A Goddard, C E Yu, J Oshima, et al.
Annales De Pediatrie|January 1, 1990
[An example of detection of heterozygotes and antenatal diagnosis in four families with anhidrotic ectodermal dysplasia]S Szpiro-Tapia, J Kaplan, A Pelet, et al.
Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.
American Journal of Human Genetics|February 1, 1995
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian familiesA Elbaz, J Vale-Santos, K Jurkat-Rott, et al.
Genomics|October 1, 1994
Homozygosity mapping of the Werner syndrome locus (WRN)J Nakura, E M Wijsman, T Miki, et al.
American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.
American Journal of Medical Genetics|March 9, 1999
Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenariansE Castro, C E Ogburn, K E Hunt, et al.
Pageof 12