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Liehr

Showing results (911-920 of 1,099) with videos related to

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European Journal of Medical Genetics|February 15, 2011
Characterization of sSMC by FISH and molecular techniquesFrenny Sheth, Joris Andrieux, Elisabeth Ewers, et al.
European Journal of Medical Genetics|April 21, 2009
Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndromeAnna D Polityko, Olga M Khurs, Anna I Kulpanovich, et al.
Oncoimmunology|March 24, 2026
Sex determines the natural killer cell-mediated immunity against pancreatic cancerElise Arlt, Nadine Bley, Alexander Rausch, et al.
American Journal of Medical Genetics. Part A|February 27, 2026
Genotype-Phenotype Correlation Through Breakpoint Characterization of a Genomically Balanced Complex Chromosomal Rearrangement Using Long Read SequencingFrenny Sheth, Jhanvi Shah, Mamta Muranjan, et al.
Molecular Medicine Reports|October 18, 2017
Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridizationZoe Papadopoulou, Ioannis Papoulidis, Stavros Sifakis, et al.
BMC Psychiatry|April 17, 2020
Non-contact monitoring of agitation and use of a sheltering device in patients with dementia in emergency departments: a feasibility studyLisa Kroll, Nikolaus Böhning, Heidi Müßigbrodt, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequencesJohn C K Barber, N Simon Thomas, Morag N Collinson, et al.
Genes|November 21, 2020
Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus <i>Harttia</i> (Teleostei, Siluriformes)Geize Aparecida Deon, Larissa Glugoski, Marcelo Ricardo Vicari, et al.
Nuklearmedizin. Nuclear Medicine|September 30, 2016
Detection of obstructive uropathy and assessment of differential renal function using two functional magnetic resonance urography tools. A comparison with diuretic renal scintigraphy in infants and childrenPhilipp Genseke, Julian M M Rogasch, Ingo G Steffen, et al.
Cancer Genetics and Cytogenetics|August 12, 2009
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21Amanda Faria de Figueiredo, Hasmik Mkrtchyan, Thomas Liehr, et al.
Pageof 110

Showing results (911-920 of 1,099) with videos related to

Sort By:
Pageof 110
European Journal of Medical Genetics|February 15, 2011
Characterization of sSMC by FISH and molecular techniquesFrenny Sheth, Joris Andrieux, Elisabeth Ewers, et al.
European Journal of Medical Genetics|April 21, 2009
Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndromeAnna D Polityko, Olga M Khurs, Anna I Kulpanovich, et al.
Oncoimmunology|March 24, 2026
Sex determines the natural killer cell-mediated immunity against pancreatic cancerElise Arlt, Nadine Bley, Alexander Rausch, et al.
American Journal of Medical Genetics. Part A|February 27, 2026
Genotype-Phenotype Correlation Through Breakpoint Characterization of a Genomically Balanced Complex Chromosomal Rearrangement Using Long Read SequencingFrenny Sheth, Jhanvi Shah, Mamta Muranjan, et al.
Molecular Medicine Reports|October 18, 2017
Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridizationZoe Papadopoulou, Ioannis Papoulidis, Stavros Sifakis, et al.
BMC Psychiatry|April 17, 2020
Non-contact monitoring of agitation and use of a sheltering device in patients with dementia in emergency departments: a feasibility studyLisa Kroll, Nikolaus Böhning, Heidi Müßigbrodt, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequencesJohn C K Barber, N Simon Thomas, Morag N Collinson, et al.
Genes|November 21, 2020
Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus <i>Harttia</i> (Teleostei, Siluriformes)Geize Aparecida Deon, Larissa Glugoski, Marcelo Ricardo Vicari, et al.
Nuklearmedizin. Nuclear Medicine|September 30, 2016
Detection of obstructive uropathy and assessment of differential renal function using two functional magnetic resonance urography tools. A comparison with diuretic renal scintigraphy in infants and childrenPhilipp Genseke, Julian M M Rogasch, Ingo G Steffen, et al.
Cancer Genetics and Cytogenetics|August 12, 2009
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21Amanda Faria de Figueiredo, Hasmik Mkrtchyan, Thomas Liehr, et al.
Pageof 110