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Thomas Liehr

Showing results (221-230 of 586) with videos related to

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Life Sciences|May 15, 2021
Identification of novel drug resistance mechanisms by genomic and transcriptomic profiling of glioblastoma cells with mutation-activated EGFROnat Kadioglu, Mohamed E M Saeed, Nuha Mahmoud, et al.
BMC Research Notes|January 4, 2016
20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literatureSaadia Amasdl, Abdelhafid Natiq, Aziza Sbiti, et al.
Molecular Cytogenetics|March 15, 2012
Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogeneticsElisabeth Klein, Marina Manvelyan, Isabella Simonyan, et al.
European Journal of Medical Genetics|August 2, 2005
Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar casesThomas Liehr, Elke Brude, Gabriele Gillessen-Kaesbach, et al.
The Journal of Heredity|April 3, 2016
W Chromosome Dynamics in Triportheus Species (Characiformes, Triportheidae): An Ongoing Process Narrated by Repetitive SequencesCassia Fernanda Yano, Luiz Antônio Carlos Bertollo, Thomas Liehr, et al.
Molecular Cytogenetics|May 13, 2022
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypesNaomi Baba, Anna Lengyel, Eva Pinti, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|June 4, 2002
Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?Alma Kuechler, Susann Neubauer, Gerhard G Grabenbauer, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|July 2, 2003
Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISHAlma Kuechler, Mareike Dreidax, Steffi U Pigorsch, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Genotype/phenotype analysis in a patient with pure and complete trisomy 12pWalter Zumkeller, Marianne Volleth, Petra Muschke, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injectionAlma Kuechler, Monika Ziegler, Cornelia Blank, et al.
Pageof 59

Showing results (221-230 of 586) with videos related to

Sort By:
Pageof 59
Life Sciences|May 15, 2021
Identification of novel drug resistance mechanisms by genomic and transcriptomic profiling of glioblastoma cells with mutation-activated EGFROnat Kadioglu, Mohamed E M Saeed, Nuha Mahmoud, et al.
BMC Research Notes|January 4, 2016
20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literatureSaadia Amasdl, Abdelhafid Natiq, Aziza Sbiti, et al.
Molecular Cytogenetics|March 15, 2012
Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogeneticsElisabeth Klein, Marina Manvelyan, Isabella Simonyan, et al.
European Journal of Medical Genetics|August 2, 2005
Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar casesThomas Liehr, Elke Brude, Gabriele Gillessen-Kaesbach, et al.
The Journal of Heredity|April 3, 2016
W Chromosome Dynamics in Triportheus Species (Characiformes, Triportheidae): An Ongoing Process Narrated by Repetitive SequencesCassia Fernanda Yano, Luiz Antônio Carlos Bertollo, Thomas Liehr, et al.
Molecular Cytogenetics|May 13, 2022
Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypesNaomi Baba, Anna Lengyel, Eva Pinti, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|June 4, 2002
Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?Alma Kuechler, Susann Neubauer, Gerhard G Grabenbauer, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|July 2, 2003
Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISHAlma Kuechler, Mareike Dreidax, Steffi U Pigorsch, et al.
American Journal of Medical Genetics. Part A|August 25, 2004
Genotype/phenotype analysis in a patient with pure and complete trisomy 12pWalter Zumkeller, Marianne Volleth, Petra Muschke, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 8, 2005
A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injectionAlma Kuechler, Monika Ziegler, Cornelia Blank, et al.
Pageof 59