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American Journal of Human Genetics
|
October 9, 2002
The DNA-based structure of human chromosome 5 in interphase
Johannes Lemke, Jan Claussen, Susanne Michel, et al.
Journal of Applied Genetics
|
May 1, 2012
How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set
Ahmed B Hamid, Katharina Kreskowski, Anja Weise, et al.
European Journal of Medical Genetics
|
September 24, 2005
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype
Joris Robert Vermeesch, Cindy Melotte, Ivo Salden, et al.
Aktuelle Urologie
|
July 27, 2013
[High-intensity focussed ultrasound in low-risk prostate cancer - oncological outcome and postinterventional quality of life of an inexperienced therapy centre in comparison with an experienced therapy centre]
D Baumunk, C Andersen, U Heile, et al.
BMC Evolutionary Biology
|
March 10, 2019
Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae): a case of chromosomal speciation?
Weerayuth Supiwong, Krit Pinthong, Kriengkrai Seetapan, et al.
Cardiovascular and Interventional Radiology
|
August 16, 2012
Short- and mid-term effects of irreversible electroporation on normal renal tissue: an animal model
J J Wendler, M Porsch, S Hühne, et al.
BMC Ecology and Evolution
|
March 18, 2025
Repetitive DNAs and differentiation of the ZZ/ZW sex chromosome system in the combtail fish Belontia hasselti (Perciformes: Osphronemidae)
Alan Moura de Oliveira, Geize Aparecida Deon, Alexandr Sember, et al.
Cytogenetic and Genome Research
|
July 3, 2013
A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification
R S Guilherme, M C S P Cernach, T E Sfakianakis, et al.
European Journal of Human Genetics : EJHG
|
February 1, 2019
Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes
Mariana Moysés-Oliveira, Adriana Di-Battista, Malú Zamariolli, et al.
European Journal of Human Genetics : EJHG
|
August 4, 2005
Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level
John C K Barber, Viv Maloney, Edward J Hollox, et al.
Page
of 110
Search research articles
Search
Showing results (921-930 of 1,099) with videos related to
Sort By:
Page
of 110
American Journal of Human Genetics
|
October 9, 2002
The DNA-based structure of human chromosome 5 in interphase
Johannes Lemke, Jan Claussen, Susanne Michel, et al.
Journal of Applied Genetics
|
May 1, 2012
How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set
Ahmed B Hamid, Katharina Kreskowski, Anja Weise, et al.
European Journal of Medical Genetics
|
September 24, 2005
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype
Joris Robert Vermeesch, Cindy Melotte, Ivo Salden, et al.
Aktuelle Urologie
|
July 27, 2013
[High-intensity focussed ultrasound in low-risk prostate cancer - oncological outcome and postinterventional quality of life of an inexperienced therapy centre in comparison with an experienced therapy centre]
D Baumunk, C Andersen, U Heile, et al.
BMC Evolutionary Biology
|
March 10, 2019
Karyotype diversity and evolutionary trends in the Asian swamp eel Monopterus albus (Synbranchiformes, Synbranchidae): a case of chromosomal speciation?
Weerayuth Supiwong, Krit Pinthong, Kriengkrai Seetapan, et al.
Cardiovascular and Interventional Radiology
|
August 16, 2012
Short- and mid-term effects of irreversible electroporation on normal renal tissue: an animal model
J J Wendler, M Porsch, S Hühne, et al.
BMC Ecology and Evolution
|
March 18, 2025
Repetitive DNAs and differentiation of the ZZ/ZW sex chromosome system in the combtail fish Belontia hasselti (Perciformes: Osphronemidae)
Alan Moura de Oliveira, Geize Aparecida Deon, Alexandr Sember, et al.
Cytogenetic and Genome Research
|
July 3, 2013
A complex chromosome rearrangement involving four chromosomes, nine breakpoints and a cryptic 0.6-Mb deletion in a boy with cerebellar hypoplasia and defects in skull ossification
R S Guilherme, M C S P Cernach, T E Sfakianakis, et al.
European Journal of Human Genetics : EJHG
|
February 1, 2019
Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes
Mariana Moysés-Oliveira, Adriana Di-Battista, Malú Zamariolli, et al.
European Journal of Human Genetics : EJHG
|
August 4, 2005
Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level
John C K Barber, Viv Maloney, Edward J Hollox, et al.
Page
of 110