Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

W Parson

Showing results (151-160 of 194) with videos related to

Pageof 20
Sort By:
Forensic Science International. Genetics|May 22, 2016
Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™M Eduardoff, T E Gross, C Santos, et al.
Forensic Science International|September 9, 2000
Is it possible to differentiate mtDNA by means of HVIII in samples that cannot be distinguished by sequencing the HVI and HVII regions?S Lutz, H Wittig, H J Weisser, et al.
Journal of the Neurological Sciences|July 17, 2010
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutationsDong-Hui Chen, Wendy H Raskind, William W Parson, et al.
Forensic Science International. Genetics|August 7, 2012
DNA commission of the International Society of Forensic Genetics: Recommendations on the evaluation of STR typing results that may include drop-out and/or drop-in using probabilistic methodsP Gill, L Gusmão, H Haned, et al.
Forensic Science International|January 1, 1999
Reproducibility of mtDNA analysis between laboratories: a report of the European DNA Profiling Group (EDNAP)A Carracedo, E D'Aloja, B Dupuy, et al.
Neurology|August 15, 2001
Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphismW D Graf, A S Unis, C M Yates, et al.
Forensic Science International. Genetics|March 15, 2016
D5S2500 is an ambiguously characterized STR: Identification and description of forensic microsatellites in the genomics ageC Phillips, W Parson, J Amigo, et al.
Forensic Science International. Genetics|August 14, 2014
DNA Commission of the International Society for Forensic Genetics: revised and extended guidelines for mitochondrial DNA typingW Parson, L Gusmão, D R Hares, et al.
Frontiers in Neurology|September 11, 2023
Quantitative assessment of collateral time on perfusion computed tomography in acute ischemic stroke patientsYao Xu, Jianhong Yang, Xiang Gao, et al.
British Journal of Cancer|November 24, 2011
Elevated mRNA expression of CHAC1 splicing variants is associated with poor outcome for breast and ovarian cancer patientsG Goebel, R Berger, A M Strasak, et al.
Pageof 20

Showing results (151-160 of 194) with videos related to

Sort By:
Pageof 20
Forensic Science International. Genetics|May 22, 2016
Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™M Eduardoff, T E Gross, C Santos, et al.
Forensic Science International|September 9, 2000
Is it possible to differentiate mtDNA by means of HVIII in samples that cannot be distinguished by sequencing the HVI and HVII regions?S Lutz, H Wittig, H J Weisser, et al.
Journal of the Neurological Sciences|July 17, 2010
A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: phenotypic spectrum and structural study of FHL1 mutationsDong-Hui Chen, Wendy H Raskind, William W Parson, et al.
Forensic Science International. Genetics|August 7, 2012
DNA commission of the International Society of Forensic Genetics: Recommendations on the evaluation of STR typing results that may include drop-out and/or drop-in using probabilistic methodsP Gill, L Gusmão, H Haned, et al.
Forensic Science International|January 1, 1999
Reproducibility of mtDNA analysis between laboratories: a report of the European DNA Profiling Group (EDNAP)A Carracedo, E D'Aloja, B Dupuy, et al.
Neurology|August 15, 2001
Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphismW D Graf, A S Unis, C M Yates, et al.
Forensic Science International. Genetics|March 15, 2016
D5S2500 is an ambiguously characterized STR: Identification and description of forensic microsatellites in the genomics ageC Phillips, W Parson, J Amigo, et al.
Forensic Science International. Genetics|August 14, 2014
DNA Commission of the International Society for Forensic Genetics: revised and extended guidelines for mitochondrial DNA typingW Parson, L Gusmão, D R Hares, et al.
Frontiers in Neurology|September 11, 2023
Quantitative assessment of collateral time on perfusion computed tomography in acute ischemic stroke patientsYao Xu, Jianhong Yang, Xiang Gao, et al.
British Journal of Cancer|November 24, 2011
Elevated mRNA expression of CHAC1 splicing variants is associated with poor outcome for breast and ovarian cancer patientsG Goebel, R Berger, A M Strasak, et al.
Pageof 20