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 (811-820 of 1,099) with videos related to

Pageof 110
Sort By:
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangementsT Liehr, N Kosayakova, J Schröder, et al.
Frontiers in Cell and Developmental Biology|April 5, 2021
Spatial Learning Is Impaired in Male Pubertal Rats Following Neonatal Daily but Not Randomly Spaced Maternal DeprivationEmily T Stoneham, Daniel G McHail, Sabina Samipour-Biel, et al.
American Journal of Medical Genetics. Part A|August 15, 2006
Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCRDiana Mitter, Karin Buiting, Ferdinand von Eggeling, et al.
Nursing Research|May 15, 2007
Behavioral therapies trials: a case exampleMarianne T Marcus, Patricia R Liehr, Joy Schmitz, et al.
Molecular Cytogenetics|January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics|November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case reportEmmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Chromosoma|July 26, 2023
Cross-species chromosome painting and repetitive DNA mapping illuminate the karyotype evolution in true crocodiles (Crocodylidae)Vanessa Sales-Oliveira, Marie Altmanová, Václav Gvoždík, et al.
Cancer Genetics|January 31, 2012
Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinomaClaudia Backsch, Birgit Pauly, Melanie Liesenfeld, et al.
Molecular Cytogenetics|November 14, 2009
A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case reportFrenny Sheth, Elisabeth Ewers, Nadezda Kosyakova, et al.
Bulletin of Experimental Biology and Medicine|November 21, 2007
Chromosome variability of human multipotent mesenchymal stromal cellsN P Bochkov, E S Voronina, N V Kosyakova, et al.
Pageof 110

Showing results (811-820 of 1,099) with videos related to

Sort By:
Pageof 110
Balkan Journal of Medical Genetics : BJMG|September 21, 2013
Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangementsT Liehr, N Kosayakova, J Schröder, et al.
Frontiers in Cell and Developmental Biology|April 5, 2021
Spatial Learning Is Impaired in Male Pubertal Rats Following Neonatal Daily but Not Randomly Spaced Maternal DeprivationEmily T Stoneham, Daniel G McHail, Sabina Samipour-Biel, et al.
American Journal of Medical Genetics. Part A|August 15, 2006
Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCRDiana Mitter, Karin Buiting, Ferdinand von Eggeling, et al.
Nursing Research|May 15, 2007
Behavioral therapies trials: a case exampleMarianne T Marcus, Patricia R Liehr, Joy Schmitz, et al.
Molecular Cytogenetics|January 9, 2009
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal maleSofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, et al.
Molecular Cytogenetics|November 19, 2008
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case reportEmmanouil Manolakos, Nadezda Kosyakova, Loreta Thomaidis, et al.
Chromosoma|July 26, 2023
Cross-species chromosome painting and repetitive DNA mapping illuminate the karyotype evolution in true crocodiles (Crocodylidae)Vanessa Sales-Oliveira, Marie Altmanová, Václav Gvoždík, et al.
Cancer Genetics|January 31, 2012
Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinomaClaudia Backsch, Birgit Pauly, Melanie Liesenfeld, et al.
Molecular Cytogenetics|November 14, 2009
A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case reportFrenny Sheth, Elisabeth Ewers, Nadezda Kosyakova, et al.
Bulletin of Experimental Biology and Medicine|November 21, 2007
Chromosome variability of human multipotent mesenchymal stromal cellsN P Bochkov, E S Voronina, N V Kosyakova, et al.
Pageof 110