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Jonson

Showing results (561-570 of 622) with videos related to

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The Journal of Pathology|January 17, 2002
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study GroupGiovanni Tallini, Howard Dorfman, Peter Brys, et al.
Physical Review Letters|September 26, 2012
Improved limit on direct α decay of the Hoyle stateO S Kirsebom, M Alcorta, M J G Borge, et al.
The Journal of Pathology|November 27, 2023
Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathwayKarim H Saba, Valeria Difilippo, Michal Kovac, et al.
Nature Genetics|June 6, 2018
Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancerJenny Karlsson, Anders Valind, Linda Holmquist Mengelbier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
PREPL deficiency: delineation of the phenotype and development of a functional blood assayLuc Régal, Emma Mårtensson, Isabelle Maystadt, et al.
Annals of Clinical and Translational Neurology|August 3, 2024
Protein-extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregationJohanna Ranta-Aho, Kevin J Felice, Per Harald Jonson, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
BiomarkersStefania Pezzoli, Alexis P Oddi, Ganna Blazhenets, et al.
Nature Genetics|February 28, 2012
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophyJaakko Sarparanta, Per Harald Jonson, Christelle Golzio, et al.
Environmental Health Perspectives|November 6, 2018
Estimates of the Global Burden of Ambient <math> </math>, Ozone, and <math> </math> on Asthma Incidence and Emergency Room VisitsSusan C Anenberg, Daven K Henze, Veronica Tinney, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Pageof 63

Showing results (561-570 of 622) with videos related to

Sort By:
Pageof 63
The Journal of Pathology|January 17, 2002
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study GroupGiovanni Tallini, Howard Dorfman, Peter Brys, et al.
Physical Review Letters|September 26, 2012
Improved limit on direct α decay of the Hoyle stateO S Kirsebom, M Alcorta, M J G Borge, et al.
The Journal of Pathology|November 27, 2023
Disruption of the TP53 locus in osteosarcoma leads to TP53 promoter gene fusions and restoration of parts of the TP53 signalling pathwayKarim H Saba, Valeria Difilippo, Michal Kovac, et al.
Nature Genetics|June 6, 2018
Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancerJenny Karlsson, Anders Valind, Linda Holmquist Mengelbier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2017
PREPL deficiency: delineation of the phenotype and development of a functional blood assayLuc Régal, Emma Mårtensson, Isabelle Maystadt, et al.
Annals of Clinical and Translational Neurology|August 3, 2024
Protein-extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregationJohanna Ranta-Aho, Kevin J Felice, Per Harald Jonson, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
BiomarkersStefania Pezzoli, Alexis P Oddi, Ganna Blazhenets, et al.
Nature Genetics|February 28, 2012
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophyJaakko Sarparanta, Per Harald Jonson, Christelle Golzio, et al.
Environmental Health Perspectives|November 6, 2018
Estimates of the Global Burden of Ambient <math> </math>, Ozone, and <math> </math> on Asthma Incidence and Emergency Room VisitsSusan C Anenberg, Daven K Henze, Veronica Tinney, et al.
European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.
Pageof 63