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 (1091-1100 of 1,099) with videos related to

Pageof 110
Sort By:
You have reached the last page of results.This site can display upto 1,099 results.
International Journal of Molecular Medicine|May 29, 2008
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literatureMarina Manvelyan, Mariluce Riegel, Monica Santos, et al.
Molecular Cytogenetics|April 4, 2013
Heteromorphic variants of chromosome 9Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, et al.
Cell|December 7, 2015
Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived FishKathrin Reichwald, Andreas Petzold, Philipp Koch, et al.
Current Biology : CB|September 8, 2021
A supernumerary "B-sex" chromosome drives male sex determination in the Pachón cavefish, Astyanax mexicanusBoudjema Imarazene, Kang Du, Séverine Beille, et al.
European Journal of Human Genetics : EJHG|May 16, 2022
Recommendations for whole genome sequencing in diagnostics for rare diseasesErika Souche, Sergi Beltran, Erwin Brosens, et al.
American Journal of Human Genetics|August 30, 2016
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human GenomeRicky S Joshi, Paras Garg, Noah Zaitlen, et al.
Human Mutation|December 2, 2017
Inactivation of AMMECR1 is associated with growth, bone, and heart alterationsMariana Moysés-Oliveira, Giuliana Giannuzzi, Richard J Fish, et al.
Nature Genetics|May 12, 2015
PDE3A mutations cause autosomal dominant hypertension with brachydactylyPhilipp G Maass, Atakan Aydin, Friedrich C Luft, et al.
American Journal of Medical Genetics. Part A|November 17, 2023
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited casesGuillaume Jedraszak, Florence Jobic, Aline Receveur, et al.
Pageof 110

Showing results (1091-1100 of 1,099) with videos related to

Sort By:
Pageof 110
You have reached the last page of results.This site can display upto 1,099 results.
International Journal of Molecular Medicine|May 29, 2008
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literatureMarina Manvelyan, Mariluce Riegel, Monica Santos, et al.
Molecular Cytogenetics|April 4, 2013
Heteromorphic variants of chromosome 9Nadezda Kosyakova, Ani Grigorian, Thomas Liehr, et al.
Cell|December 7, 2015
Insights into Sex Chromosome Evolution and Aging from the Genome of a Short-Lived FishKathrin Reichwald, Andreas Petzold, Philipp Koch, et al.
Current Biology : CB|September 8, 2021
A supernumerary "B-sex" chromosome drives male sex determination in the Pachón cavefish, Astyanax mexicanusBoudjema Imarazene, Kang Du, Séverine Beille, et al.
European Journal of Human Genetics : EJHG|May 16, 2022
Recommendations for whole genome sequencing in diagnostics for rare diseasesErika Souche, Sergi Beltran, Erwin Brosens, et al.
American Journal of Human Genetics|August 30, 2016
DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human GenomeRicky S Joshi, Paras Garg, Noah Zaitlen, et al.
Human Mutation|December 2, 2017
Inactivation of AMMECR1 is associated with growth, bone, and heart alterationsMariana Moysés-Oliveira, Giuliana Giannuzzi, Richard J Fish, et al.
Nature Genetics|May 12, 2015
PDE3A mutations cause autosomal dominant hypertension with brachydactylyPhilipp G Maass, Atakan Aydin, Friedrich C Luft, et al.
American Journal of Medical Genetics. Part A|November 17, 2023
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited casesGuillaume Jedraszak, Florence Jobic, Aline Receveur, et al.
Pageof 110