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

Liehr

Showing results (971-980 of 1,099) with videos related to

Pageof 110
Sort By:
European Journal of Human Genetics : EJHG|July 26, 2012
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2John C K Barber, Victoria Hall, Viv K Maloney, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2015
X-linked intellectual disability related genes disrupted by balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, et al.
Molecular Cytogenetics|February 20, 2010
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new familiesJohn Ck Barber, Dave Bunyan, Merryl Curtis, et al.
Molecular Cytogenetics|April 29, 2016
Chromosomes in a genome-wise order: evidence for metaphase architectureAnja Weise, Samarth Bhatt, Katja Piaszinski, et al.
Cardiovascular and Interventional Radiology|September 21, 2017
Upper-Urinary-Tract Effects After Irreversible Electroporation (IRE) of Human Localised Renal-Cell Carcinoma (RCC) in the IRENE Pilot Phase 2a Ablate-and-Resect StudyJ J Wendler, M Pech, J Köllermann, et al.
Journal of Internal Medicine|May 17, 2008
Endoscopy in Barrett's oesophagus: adherence to standards and neoplasia detection in the community practice versus hospital settingH Pohl, J Aschenbeck, R Drossel, et al.
Genetics in Medicine Open|May 28, 2026
Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencingMei Ling Chong, Bruna Burssed, Chen Zhao, et al.
Journal of the National Cancer Institute. Monographs|August 30, 2000
Tissue-specific synthesis and oxidative metabolism of estrogensC R Jefcoate, J G Liehr, R J Santen, et al.
Molecular Cytogenetics|September 16, 2017
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndromeDaiane Correa de Souza, Amanda Faria de Figueiredo, Daniela R Ney Garcia, et al.
Molecular Cytogenetics|August 11, 2015
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemiaAmanda Faria de Figueiredo, Roberto Rodrigues Capela de Matos, Moneeb A K Othman, et al.
Pageof 110

Showing results (971-980 of 1,099) with videos related to

Sort By:
Pageof 110
European Journal of Human Genetics : EJHG|July 26, 2012
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2John C K Barber, Victoria Hall, Viv K Maloney, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2015
X-linked intellectual disability related genes disrupted by balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, et al.
Molecular Cytogenetics|February 20, 2010
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new familiesJohn Ck Barber, Dave Bunyan, Merryl Curtis, et al.
Molecular Cytogenetics|April 29, 2016
Chromosomes in a genome-wise order: evidence for metaphase architectureAnja Weise, Samarth Bhatt, Katja Piaszinski, et al.
Cardiovascular and Interventional Radiology|September 21, 2017
Upper-Urinary-Tract Effects After Irreversible Electroporation (IRE) of Human Localised Renal-Cell Carcinoma (RCC) in the IRENE Pilot Phase 2a Ablate-and-Resect StudyJ J Wendler, M Pech, J Köllermann, et al.
Journal of Internal Medicine|May 17, 2008
Endoscopy in Barrett's oesophagus: adherence to standards and neoplasia detection in the community practice versus hospital settingH Pohl, J Aschenbeck, R Drossel, et al.
Genetics in Medicine Open|May 28, 2026
Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencingMei Ling Chong, Bruna Burssed, Chen Zhao, et al.
Journal of the National Cancer Institute. Monographs|August 30, 2000
Tissue-specific synthesis and oxidative metabolism of estrogensC R Jefcoate, J G Liehr, R J Santen, et al.
Molecular Cytogenetics|September 16, 2017
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndromeDaiane Correa de Souza, Amanda Faria de Figueiredo, Daniela R Ney Garcia, et al.
Molecular Cytogenetics|August 11, 2015
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemiaAmanda Faria de Figueiredo, Roberto Rodrigues Capela de Matos, Moneeb A K Othman, et al.
Pageof 110