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

T Liehr

Showing results (181-190 of 192) with videos related to

Pageof 20
Sort By:
Molecular Syndromology|November 1, 2012
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi AnemiaA Serra, K Eirich, A K Winkler, et al.
Arthritis Research|September 11, 2001
Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseasesR W Kinne, T Liehr, V Beensen, et al.
Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.
Cancer Genetics|January 2, 2022
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21R R Capela de Matos, Mak Othman, G M Ferreira, et al.
Cytogenetic and Genome Research|April 11, 2012
Tetrasomy 9p mosaicism associated with a normal phenotype in two casesI Papoulidis, M Kontodiou, M Tzimina, et al.
Cytogenetic and Genome Research|November 9, 2005
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlationT Liehr, K Mrasek, A Weise, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Acta Haematologica|February 1, 2013
An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemiaR R C Matos, H Mkrtchyan, B A S Amaral, et al.
Genetics and Molecular Research : GMR|May 8, 2010
Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndromeP Burégio-Frota, L Valença, G F Leal, et al.
Molecular Medicine Reports|April 8, 2011
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridizationE Manolakos, K Kefalas, R Neroutsou, et al.
Pageof 20

Showing results (181-190 of 192) with videos related to

Sort By:
Pageof 20
Molecular Syndromology|November 1, 2012
Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi AnemiaA Serra, K Eirich, A K Winkler, et al.
Arthritis Research|September 11, 2001
Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseasesR W Kinne, T Liehr, V Beensen, et al.
Journal of Medical Genetics|January 1, 1997
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descentV Timmerman, B Rautenstrauss, L T Reiter, et al.
Cancer Genetics|January 2, 2022
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21R R Capela de Matos, Mak Othman, G M Ferreira, et al.
Cytogenetic and Genome Research|April 11, 2012
Tetrasomy 9p mosaicism associated with a normal phenotype in two casesI Papoulidis, M Kontodiou, M Tzimina, et al.
Cytogenetic and Genome Research|November 9, 2005
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlationT Liehr, K Mrasek, A Weise, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Acta Haematologica|February 1, 2013
An unusual cytogenetic rearrangement originating from two different abnormalities in chromosome 6 in a child with acute promyelocytic leukemiaR R C Matos, H Mkrtchyan, B A S Amaral, et al.
Genetics and Molecular Research : GMR|May 8, 2010
Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndromeP Burégio-Frota, L Valença, G F Leal, et al.
Molecular Medicine Reports|April 8, 2011
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridizationE Manolakos, K Kefalas, R Neroutsou, et al.
Pageof 20