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Thomas Liehr

Showing results (251-260 of 586) with videos related to

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BMC Evolutionary Biology|July 2, 2011
Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishesMarcelo B Cioffi, Antonio Sánchez, Juan A Marchal, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 28, 2012
Characterization of three small supernumerary marker chromosomes (sSMC) in humansJian Ou, Wei Wang, Thomas Liehr, et al.
Prenatal Diagnosis|December 23, 2004
Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2)Thomas Liehr, Anita Heller, Karl-Heinz Eichhorn, et al.
Hematology, Transfusion and Cell Therapy|February 23, 2019
Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndromeMaria Luiza Rocha da Rosa Borges, Eliane Maria Soares-Ventura, Thomas Liehr, et al.
Frontiers in Genetics|April 1, 2022
First Comprehensive Characterization of Phayre's Leaf-Monkey (<i>Trachypithecus phayrei</i>) KaryotypeXiaobo Fan, Krit Pinthong, Edivaldo H C de Oliveira, et al.
Molecular Cytogenetics|July 22, 2010
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanationSusana I Ferreira, Eunice Matoso, Marta Pinto, et al.
Genes|June 26, 2025
Results of Chromosomal Microarray Need to Always Be Checked by (Molecular) Cytogenetics-Even If They Seem to Be Simple DeletionsThomas Liehr, Sylke Singer, Ulrike Mau-Holzmann, et al.
Journal of Advanced Research|July 3, 2026
Involvement of cyclins in the pathogenesis of cancerMohammad Taheri, Zeinab Shirvani-Farsani, Bashdar Mahmud Hussen, et al.
The Journal of Obstetrics and Gynaecology Research|May 25, 2010
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: molecular cytogenetic analysis and review of the literatureEmmanouil Manolakos, Panagiotis Peitsidis, Makarios Eleftheriades, et al.
European Journal of Medical Genetics|September 10, 2010
Duplication 4q associated with chronic cholestatic changes in liver biopsyOdul Egritas, Busranur Cavdarli, Buket Dalgic, et al.
Pageof 59

Showing results (251-260 of 586) with videos related to

Sort By:
Pageof 59
BMC Evolutionary Biology|July 2, 2011
Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishesMarcelo B Cioffi, Antonio Sánchez, Juan A Marchal, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 28, 2012
Characterization of three small supernumerary marker chromosomes (sSMC) in humansJian Ou, Wei Wang, Thomas Liehr, et al.
Prenatal Diagnosis|December 23, 2004
Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2)Thomas Liehr, Anita Heller, Karl-Heinz Eichhorn, et al.
Hematology, Transfusion and Cell Therapy|February 23, 2019
Minimally differentiated acute myeloid leukemia with ring/marker derived from chromosome 7 in a child with Down syndromeMaria Luiza Rocha da Rosa Borges, Eliane Maria Soares-Ventura, Thomas Liehr, et al.
Frontiers in Genetics|April 1, 2022
First Comprehensive Characterization of Phayre's Leaf-Monkey (<i>Trachypithecus phayrei</i>) KaryotypeXiaobo Fan, Krit Pinthong, Edivaldo H C de Oliveira, et al.
Molecular Cytogenetics|July 22, 2010
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanationSusana I Ferreira, Eunice Matoso, Marta Pinto, et al.
Genes|June 26, 2025
Results of Chromosomal Microarray Need to Always Be Checked by (Molecular) Cytogenetics-Even If They Seem to Be Simple DeletionsThomas Liehr, Sylke Singer, Ulrike Mau-Holzmann, et al.
Journal of Advanced Research|July 3, 2026
Involvement of cyclins in the pathogenesis of cancerMohammad Taheri, Zeinab Shirvani-Farsani, Bashdar Mahmud Hussen, et al.
The Journal of Obstetrics and Gynaecology Research|May 25, 2010
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: molecular cytogenetic analysis and review of the literatureEmmanouil Manolakos, Panagiotis Peitsidis, Makarios Eleftheriades, et al.
European Journal of Medical Genetics|September 10, 2010
Duplication 4q associated with chronic cholestatic changes in liver biopsyOdul Egritas, Busranur Cavdarli, Buket Dalgic, et al.
Pageof 59