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 (101-110 of 586) with videos related to

Pageof 59
Sort By:
Cytogenetic and Genome Research|September 24, 2015
Small Supernumerary Marker Chromosomes in Human InfertilityNarjes Armanet, Lucie Tosca, Sophie Brisset, et al.
F1000Research|May 24, 2023
Case Report: Identification of likely recurrent <i>CEP290</i> mutation in a child with Joubert syndrome and cerebello-retinal-renal featuresLidvana Spahiu, John A Sayer, Emir Behluli, et al.
Biomolecular Engineering|July 14, 2007
Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrityIvan Y Iourov, Thomas Liehr, Svetlana G Vorsanova, et al.
Molecular Cytogenetics|March 18, 2010
A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3Walid Al Achkar, Abdulsamad Wafa, Hasmik Mkrtchyan, et al.
Oncology Letters|June 14, 2013
Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patientWalid Al-Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|September 19, 2019
Chromosome Microdissection on Semi-Archived MaterialAhmed B Hamid Al-Rikabi, Marcelo de Bello Cioffi, Thomas Liehr
Indian Journal of Human Genetics|June 25, 2014
Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like faciesAbdelhafid Natiq, Siham Chafai Elalaoui, Thomas Liehr, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 14, 2015
Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3)Susanne Ledig, Sabine Preisler-Adams, Susanne Morlot, et al.
Journal of Mother and Child|February 21, 2023
Joubert syndrome: Molecular basis and treatmentLidvana Spahiu, Emir Behluli, Violeta Grajçevci-Uka, et al.
Oncology Letters|September 12, 2012
A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17)Walid Al Achkar, Abdulsamad Wafa, Hasmik Mkrtchyan, et al.
Pageof 59

Showing results (101-110 of 586) with videos related to

Sort By:
Pageof 59
Cytogenetic and Genome Research|September 24, 2015
Small Supernumerary Marker Chromosomes in Human InfertilityNarjes Armanet, Lucie Tosca, Sophie Brisset, et al.
F1000Research|May 24, 2023
Case Report: Identification of likely recurrent <i>CEP290</i> mutation in a child with Joubert syndrome and cerebello-retinal-renal featuresLidvana Spahiu, John A Sayer, Emir Behluli, et al.
Biomolecular Engineering|July 14, 2007
Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrityIvan Y Iourov, Thomas Liehr, Svetlana G Vorsanova, et al.
Molecular Cytogenetics|March 18, 2010
A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3Walid Al Achkar, Abdulsamad Wafa, Hasmik Mkrtchyan, et al.
Oncology Letters|June 14, 2013
Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patientWalid Al-Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|September 19, 2019
Chromosome Microdissection on Semi-Archived MaterialAhmed B Hamid Al-Rikabi, Marcelo de Bello Cioffi, Thomas Liehr
Indian Journal of Human Genetics|June 25, 2014
Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like faciesAbdelhafid Natiq, Siham Chafai Elalaoui, Thomas Liehr, et al.
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|February 14, 2015
Premature ovarian failure caused by a heterozygous missense mutation in POF1B and a reciprocal translocation 46,X,t(X;3)(q21.1;q21.3)Susanne Ledig, Sabine Preisler-Adams, Susanne Morlot, et al.
Journal of Mother and Child|February 21, 2023
Joubert syndrome: Molecular basis and treatmentLidvana Spahiu, Emir Behluli, Violeta Grajçevci-Uka, et al.
Oncology Letters|September 12, 2012
A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17)Walid Al Achkar, Abdulsamad Wafa, Hasmik Mkrtchyan, et al.
Pageof 59