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

Thomas Liehr

Showing results (181-190 of 586) with videos related to

Pageof 59
Sort By:
Leukemia Research Reports|August 8, 2020
Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myelomaHasna Hamdaoui, Abdelhafid Natiq, Oumaima Benlarroubia, et al.
Pathology, Research and Practice|June 17, 2023
Single cell RNA-seq analysis with a systems biology approach to recognize important differentially expressed genes in pancreatic ductal adenocarcinoma compared to adjacent non-cancerous samples by targeting pancreatic endothelial cellsElena Jamali, Arash Safarzadeh, Bashdar Mahmud Hussen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 30, 2016
A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findingsBardo Wannenmacher, Diana Mitter, Franziska Kießling, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|November 8, 2021
Mucopolysaccharidosis III: Molecular basis and treatmentLidvana Spahiu, Emir Behluli, Borut Peterlin, et al.
International Journal of Oncology|March 10, 2006
Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approachesConstanze Karst, Madeleine Gross, Detlef Haase, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|May 6, 2004
Impact of various parameters in detecting chromosomal aberrations by FISH to describe radiosensitivityUlrike Keller, Alma Kuechler, Thomas Liehr, et al.
Expert Review of Molecular Diagnostics|May 14, 2009
Handling small supernumerary marker chromosomes in prenatal diagnosticsThomas Liehr, Elisabeth Ewers, Nadezda Kosyakova, et al.
Case Reports in Genetics|January 16, 2013
Gain of chromosome 4qter and loss of 5pter: an unusual case with features of cri du chat syndromeFrenny Sheth, Naresh Gohel, Thomas Liehr, et al.
Molecular Cytogenetics|March 8, 2014
X chromosome aneuploidy in the Alzheimer's disease brainYuri B Yurov, Svetlana G Vorsanova, Thomas Liehr, et al.
Clinical Dysmorphology|August 22, 2014
Partial monosomy 3q26.33-3q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case reportYavuz Şahin, Pelin Ö Kiper, Yasemin Alanay, et al.
Pageof 59

Showing results (181-190 of 586) with videos related to

Sort By:
Pageof 59
Leukemia Research Reports|August 8, 2020
Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myelomaHasna Hamdaoui, Abdelhafid Natiq, Oumaima Benlarroubia, et al.
Pathology, Research and Practice|June 17, 2023
Single cell RNA-seq analysis with a systems biology approach to recognize important differentially expressed genes in pancreatic ductal adenocarcinoma compared to adjacent non-cancerous samples by targeting pancreatic endothelial cellsElena Jamali, Arash Safarzadeh, Bashdar Mahmud Hussen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 30, 2016
A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findingsBardo Wannenmacher, Diana Mitter, Franziska Kießling, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|November 8, 2021
Mucopolysaccharidosis III: Molecular basis and treatmentLidvana Spahiu, Emir Behluli, Borut Peterlin, et al.
International Journal of Oncology|March 10, 2006
Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approachesConstanze Karst, Madeleine Gross, Detlef Haase, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|May 6, 2004
Impact of various parameters in detecting chromosomal aberrations by FISH to describe radiosensitivityUlrike Keller, Alma Kuechler, Thomas Liehr, et al.
Expert Review of Molecular Diagnostics|May 14, 2009
Handling small supernumerary marker chromosomes in prenatal diagnosticsThomas Liehr, Elisabeth Ewers, Nadezda Kosyakova, et al.
Case Reports in Genetics|January 16, 2013
Gain of chromosome 4qter and loss of 5pter: an unusual case with features of cri du chat syndromeFrenny Sheth, Naresh Gohel, Thomas Liehr, et al.
Molecular Cytogenetics|March 8, 2014
X chromosome aneuploidy in the Alzheimer's disease brainYuri B Yurov, Svetlana G Vorsanova, Thomas Liehr, et al.
Clinical Dysmorphology|August 22, 2014
Partial monosomy 3q26.33-3q27.3 presenting with intellectual disability, facial dysmorphism, and diaphragm eventration: a case reportYavuz Şahin, Pelin Ö Kiper, Yasemin Alanay, et al.
Pageof 59