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T Liehr

Showing results (121-130 of 192) with videos related to

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Journal of Intellectual Disability Research : JIDR|December 22, 2017
7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorderL Castiglia, R A Husain, I Marquardt, et al.
Cytogenetic and Genome Research|June 26, 2004
The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB)H Lehrer, A Weise, S Michel, et al.
Cytogenetic and Genome Research|March 9, 2004
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding methodA Weise, A Heller, H Starke, et al.
Cytogenetic and Genome Research|November 20, 2002
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA librariesT Liehr, A Weise, A Heller, et al.
Human Reproduction (Oxford, England)|June 6, 2006
Analysis of non-crossover bivalents in pachytene cells from 10 normal menFei Sun, M Oliver-Bonet, T Liehr, et al.
Heredity|December 22, 2016
Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae)C F Yano, L A C Bertollo, T Ezaz, et al.
Cytogenetic and Genome Research|February 24, 2007
Array painting using microdissected chromosomes to map chromosomal breakpointsL Backx, H Van Esch, C Melotte, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delayG von Beust, S M Sauter, T Liehr, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouthS Balci, B Yuksel Konuk, F Atik, et al.
Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.
Pageof 20

Showing results (121-130 of 192) with videos related to

Sort By:
Pageof 20
Journal of Intellectual Disability Research : JIDR|December 22, 2017
7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorderL Castiglia, R A Husain, I Marquardt, et al.
Cytogenetic and Genome Research|June 26, 2004
The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB)H Lehrer, A Weise, S Michel, et al.
Cytogenetic and Genome Research|March 9, 2004
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding methodA Weise, A Heller, H Starke, et al.
Cytogenetic and Genome Research|November 20, 2002
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA librariesT Liehr, A Weise, A Heller, et al.
Human Reproduction (Oxford, England)|June 6, 2006
Analysis of non-crossover bivalents in pachytene cells from 10 normal menFei Sun, M Oliver-Bonet, T Liehr, et al.
Heredity|December 22, 2016
Highly conserved Z and molecularly diverged W chromosomes in the fish genus Triportheus (Characiformes, Triportheidae)C F Yano, L A C Bertollo, T Ezaz, et al.
Cytogenetic and Genome Research|February 24, 2007
Array painting using microdissected chromosomes to map chromosomal breakpointsL Backx, H Van Esch, C Melotte, et al.
American Journal of Medical Genetics. Part A|July 12, 2005
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delayG von Beust, S M Sauter, T Liehr, et al.
Genetic Counseling (Geneva, Switzerland)|October 23, 2010
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouthS Balci, B Yuksel Konuk, F Atik, et al.
Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.
Pageof 20