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Showing results (221-230 of 284) with videos related to

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Annals of the New York Academy of Sciences|January 1, 1985
Isolation and characterization of the human fibrillar collagen genesF Ramirez, M Bernard, M L Chu, et al.
Circulation|December 1, 1994
Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophyD Annane, D Duboc, B Mazoyer, et al.
Human Molecular Genetics|July 21, 1998
Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacitiesA S Lia, H Seznec, H Hofmann-Radvanyi, et al.
Journal of Medical Genetics|February 1, 1992
A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium studyM Sarfarazi, P Tsipouras, R Del Mastro, et al.
Annales De Genetique|January 1, 1984
The structural gene for transferrin (TF) maps to 3q21----3qterC Huerre, G Uzan, K H Grzeschik, et al.
American Journal of Human Genetics|August 12, 1999
Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutationG Collod-Béroud, M Lackmy-Port-Lys, G Jondeau, et al.
Tissue Antigens|October 18, 2000
HLA-DRB1 and DQB1 genotypes in patients with insulin-dependent neonatal diabetes mellitus. A study of 13 casesE Marquis, I Le Monnier de Gouville, C Bouvattier, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.
Genomics|July 1, 1988
Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumorW H Lewis, H Yeger, L Bonetta, et al.
Genes, Chromosomes & Cancer|May 1, 1993
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a familyI Henry, J Hoovers, F Barichard, et al.
Pageof 29

Showing results (221-230 of 284) with videos related to

Sort By:
Pageof 29
Annals of the New York Academy of Sciences|January 1, 1985
Isolation and characterization of the human fibrillar collagen genesF Ramirez, M Bernard, M L Chu, et al.
Circulation|December 1, 1994
Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophyD Annane, D Duboc, B Mazoyer, et al.
Human Molecular Genetics|July 21, 1998
Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacitiesA S Lia, H Seznec, H Hofmann-Radvanyi, et al.
Journal of Medical Genetics|February 1, 1992
A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an International Consortium studyM Sarfarazi, P Tsipouras, R Del Mastro, et al.
Annales De Genetique|January 1, 1984
The structural gene for transferrin (TF) maps to 3q21----3qterC Huerre, G Uzan, K H Grzeschik, et al.
American Journal of Human Genetics|August 12, 1999
Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutationG Collod-Béroud, M Lackmy-Port-Lys, G Jondeau, et al.
Tissue Antigens|October 18, 2000
HLA-DRB1 and DQB1 genotypes in patients with insulin-dependent neonatal diabetes mellitus. A study of 13 casesE Marquis, I Le Monnier de Gouville, C Bouvattier, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization eventI Henry, A Puech, A Riesewijk, et al.
Genomics|July 1, 1988
Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumorW H Lewis, H Yeger, L Bonetta, et al.
Genes, Chromosomes & Cancer|May 1, 1993
Pericentric intrachromosomal insertion responsible for recurrence of del(11)(p13p14) in a familyI Henry, J Hoovers, F Barichard, et al.
Pageof 29