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Pekka Ellonen

Showing results (1-10 of 66) with videos related to

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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 13, 2011
TBX22 and tongue-tieTuomas Klockars, Suvi Kyttänen, Pekka Ellonen
European Journal of Human Genetics : EJHG|April 16, 2009
Genetic markers and population history: Finland revisitedJukka U Palo, Ismo Ulmanen, Matti Lukka, et al.
Forensic Science International|December 13, 2005
Triallelic patterns in STR loci used for paternity analysis: evidence for a duplication in chromosome 2 containing the TPOX STR locusMatti Lukka, Gunnar Tasa, Pekka Ellonen, et al.
Experimental Dermatology|April 3, 2014
Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencingEmma Andersson, Samuli Eldfors, Henrik Edgren, et al.
Epigenomics|November 4, 2016
Genome-wide DNA methylation in saliva and body size of adolescent girlsTrine B Rounge, Christian M Page, Maija Lepistö, et al.
Journal of the Endocrine Society|March 20, 2020
IDH1 Expression via the R132H Mutation-Specific Antibody in Adrenocortical Neoplasias-Prognostic Impact in CarcinomasMirkka Pennanen, Olli Tynninen, Soili Kytölä, et al.
Leukemia & Lymphoma|April 5, 2018
Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemiaPoojitha N Ojamies, Mika Kontro, Henrik Edgren, et al.
BMC Cancer|December 19, 2024
Differential somatic coding variant landscapes between laser microdissected luminal epithelial cells from canine mammary invasive ductal solid carcinoma and comedocarcinomaVivi Deckwirth, Sruthi Hundi, Marjo K Hytönen, et al.
Clinical Genetics|September 9, 2020
Identifying haplotypes in recessive inherited retinal dystrophies using whole-genome linked-read sequencingPauliina Repo, Reetta-Stiina Järvinen, Eeva-Marja Sankila, et al.
Clinical Immunology (Orlando, Fla.)|December 10, 2016
A novel class of somatic mutations in blood detected preferentially in CD8+ cellsMiko Valori, Lilja Jansson, Anna Kiviharju, et al.
Pageof 7

Showing results (1-10 of 66) with videos related to

Sort By:
Pageof 7
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 13, 2011
TBX22 and tongue-tieTuomas Klockars, Suvi Kyttänen, Pekka Ellonen
European Journal of Human Genetics : EJHG|April 16, 2009
Genetic markers and population history: Finland revisitedJukka U Palo, Ismo Ulmanen, Matti Lukka, et al.
Forensic Science International|December 13, 2005
Triallelic patterns in STR loci used for paternity analysis: evidence for a duplication in chromosome 2 containing the TPOX STR locusMatti Lukka, Gunnar Tasa, Pekka Ellonen, et al.
Experimental Dermatology|April 3, 2014
Novel TBL1XR1, EPHA7 and SLFN12 mutations in a Sezary syndrome patient discovered by whole exome sequencingEmma Andersson, Samuli Eldfors, Henrik Edgren, et al.
Epigenomics|November 4, 2016
Genome-wide DNA methylation in saliva and body size of adolescent girlsTrine B Rounge, Christian M Page, Maija Lepistö, et al.
Journal of the Endocrine Society|March 20, 2020
IDH1 Expression via the R132H Mutation-Specific Antibody in Adrenocortical Neoplasias-Prognostic Impact in CarcinomasMirkka Pennanen, Olli Tynninen, Soili Kytölä, et al.
Leukemia & Lymphoma|April 5, 2018
Case studies investigating genetic heterogeneity between anatomically distinct bone marrow compartments in acute myeloid leukemiaPoojitha N Ojamies, Mika Kontro, Henrik Edgren, et al.
BMC Cancer|December 19, 2024
Differential somatic coding variant landscapes between laser microdissected luminal epithelial cells from canine mammary invasive ductal solid carcinoma and comedocarcinomaVivi Deckwirth, Sruthi Hundi, Marjo K Hytönen, et al.
Clinical Genetics|September 9, 2020
Identifying haplotypes in recessive inherited retinal dystrophies using whole-genome linked-read sequencingPauliina Repo, Reetta-Stiina Järvinen, Eeva-Marja Sankila, et al.
Clinical Immunology (Orlando, Fla.)|December 10, 2016
A novel class of somatic mutations in blood detected preferentially in CD8+ cellsMiko Valori, Lilja Jansson, Anna Kiviharju, et al.
Pageof 7