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Thomas Liehr

Showing results (471-480 of 586) with videos related to

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Reproduction, Fertility, and Development|October 9, 2014
Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation caseAdriana Valéria Sales Bispo, Pollyanna Burégio-Frota, Luana Oliveira dos Santos, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangementsHeike Starke, Jörg Seidel, Wolfram Henn, et al.
Journal of Cellular and Molecular Medicine|June 16, 2022
Analysis and pharmacological modulation of senescence in human epithelial stem cellsVanessa Barbaro, Antonio Orvieto, Gualtiero Alvisi, et al.
Plos One|July 18, 2024
Comparative karyotypic study of fifteen cyprinids (Cyprinidae, Cyprininae) species. An insight into the chromosomal evolution of the tribe SystominiPhichaya Buasriyot, Francisco de Menezes Cavalcante Sassi, Nuttasuda Donbundit, et al.
The EMBO Journal|June 21, 2018
Reorganization of <i>inter-</i>chromosomal interactions in the 2q37-deletion syndromePhilipp G Maass, Anja Weise, Katharina Rittscher, et al.
Scientific Reports|September 21, 2023
Homeology of sex chromosomes in Amazonian Harttia armored catfishes supports the X-fission hypothesis for the X<sub>1</sub>X<sub>2</sub>Y sex chromosome system originFrancisco de Menezes Cavalcante Sassi, Alexandr Sember, Geize Aparecida Deon, et al.
Journal of the Association of Genetic Technologists|June 24, 2004
Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic ApproachesThomas Liehr, Angela Nietzel, Heike Starke, et al.
European Journal of Human Genetics : EJHG|July 26, 2012
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2John C K Barber, Victoria Hall, Viv K Maloney, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2015
X-linked intellectual disability related genes disrupted by balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, et al.
Molecular Cytogenetics|February 20, 2010
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new familiesJohn Ck Barber, Dave Bunyan, Merryl Curtis, et al.
Pageof 59

Showing results (471-480 of 586) with videos related to

Sort By:
Pageof 59
Reproduction, Fertility, and Development|October 9, 2014
Y chromosome in Turner syndrome: detection of hidden mosaicism and the report of a rare X;Y translocation caseAdriana Valéria Sales Bispo, Pollyanna Burégio-Frota, Luana Oliveira dos Santos, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangementsHeike Starke, Jörg Seidel, Wolfram Henn, et al.
Journal of Cellular and Molecular Medicine|June 16, 2022
Analysis and pharmacological modulation of senescence in human epithelial stem cellsVanessa Barbaro, Antonio Orvieto, Gualtiero Alvisi, et al.
Plos One|July 18, 2024
Comparative karyotypic study of fifteen cyprinids (Cyprinidae, Cyprininae) species. An insight into the chromosomal evolution of the tribe SystominiPhichaya Buasriyot, Francisco de Menezes Cavalcante Sassi, Nuttasuda Donbundit, et al.
The EMBO Journal|June 21, 2018
Reorganization of <i>inter-</i>chromosomal interactions in the 2q37-deletion syndromePhilipp G Maass, Anja Weise, Katharina Rittscher, et al.
Scientific Reports|September 21, 2023
Homeology of sex chromosomes in Amazonian Harttia armored catfishes supports the X-fission hypothesis for the X<sub>1</sub>X<sub>2</sub>Y sex chromosome system originFrancisco de Menezes Cavalcante Sassi, Alexandr Sember, Geize Aparecida Deon, et al.
Journal of the Association of Genetic Technologists|June 24, 2004
Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic ApproachesThomas Liehr, Angela Nietzel, Heike Starke, et al.
European Journal of Human Genetics : EJHG|July 26, 2012
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2John C K Barber, Victoria Hall, Viv K Maloney, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 21, 2015
X-linked intellectual disability related genes disrupted by balanced X-autosome translocationsMariana Moysés-Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, et al.
Molecular Cytogenetics|February 20, 2010
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new familiesJohn Ck Barber, Dave Bunyan, Merryl Curtis, et al.
Pageof 59