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J M Barceló

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Human Mutation|January 1, 1996
Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCRS Cheng, J M Barceló, R G Korneluk
Human Molecular Genetics|January 1, 1994
High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutationC E Neville, M S Mahadevan, J M Barceló, et al.
Human Molecular Genetics|June 1, 1993
Intergenerational stability of the myotonic dystrophy protomutationJ M Barceló, M S Mahadevan, C Tsilfidis, et al.
American Journal of Human Genetics|June 1, 1994
Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophyJ M Barceló, M Pluscauskas, A E MacKenzie, et al.
Medicina Clinica|February 4, 1989
[Unusual association of Graves' disease and Bartter's syndrome]J M Barceló Valcárcel, A El Amrani El Marini, A Montes Puertas, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2001
Human mitochondrial topoisomerase IH Zhang, J M Barceló, B Lee, et al.
American Journal of Human Genetics|March 1, 1994
Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.
Environmental Research|April 15, 2022
Non-linear models for black carbon exposure modelling using air pollution datasetsJ Rovira, J A Paredes-Ahumada, J M Barceló-Ordinas, et al.
Contact Dermatitis|October 31, 2001
Cistus ladanifer contact dermatitisJ J García-González, V Crespo, D Barber, et al.
Revista Espanola De Las Enfermedades Del Aparato Digestivo|November 1, 1987
[Diagnostic importance of ultrasonic non-visualization of the gallbladder as a sign of gallbladder disease]P Aranegui-Lasuen, F Ortiz-Flores, L T Guzmán-Tirado, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Human Mutation|January 1, 1996
Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCRS Cheng, J M Barceló, R G Korneluk
Human Molecular Genetics|January 1, 1994
High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutationC E Neville, M S Mahadevan, J M Barceló, et al.
Human Molecular Genetics|June 1, 1993
Intergenerational stability of the myotonic dystrophy protomutationJ M Barceló, M S Mahadevan, C Tsilfidis, et al.
American Journal of Human Genetics|June 1, 1994
Additive influence of maternal and offspring DM-kinase gene CTG repeat lengths in the genesis of congenital myotonic dystrophyJ M Barceló, M Pluscauskas, A E MacKenzie, et al.
Medicina Clinica|February 4, 1989
[Unusual association of Graves' disease and Bartter's syndrome]J M Barceló Valcárcel, A El Amrani El Marini, A Montes Puertas, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2001
Human mitochondrial topoisomerase IH Zhang, J M Barceló, B Lee, et al.
American Journal of Human Genetics|March 1, 1994
Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.
Environmental Research|April 15, 2022
Non-linear models for black carbon exposure modelling using air pollution datasetsJ Rovira, J A Paredes-Ahumada, J M Barceló-Ordinas, et al.
Contact Dermatitis|October 31, 2001
Cistus ladanifer contact dermatitisJ J García-González, V Crespo, D Barber, et al.
Revista Espanola De Las Enfermedades Del Aparato Digestivo|November 1, 1987
[Diagnostic importance of ultrasonic non-visualization of the gallbladder as a sign of gallbladder disease]P Aranegui-Lasuen, F Ortiz-Flores, L T Guzmán-Tirado, et al.
Pageof 2