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Udo Koehler

Showing results (11-20 of 26) with videos related to

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Cancer Biomarkers : Section a of Disease Markers|February 12, 2013
CD133 is a predictor of poor survival in head and neck squamous cell carcinomasMartin Canis, Axel Lechner, Brigitte Mack, et al.
European Journal of Pediatrics|September 19, 2009
A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosumUdo Koehler, Elke Holinski-Feder, Birgit Ertl-Wagner, et al.
Cytogenetic and Genome Research|December 10, 2023
Genome Mapping NomenclatureSarah Moore, Jean McGowan-Jordan, Adam C Smith, et al.
Genes|March 28, 2024
Optical Genome Mapping as a Potential Routine Clinical Diagnostic MethodHayk Barseghyan, Doris Eisenreich, Evgenia Lindt, et al.
Human Molecular Genetics|February 18, 2009
In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromesStefanie Bulst, Angela Abicht, Elke Holinski-Feder, et al.
Journal of Medical Genetics|June 30, 2011
Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndromeMonika Morak, Udo Koehler, Hans Konrad Schackert, et al.
European Journal of Human Genetics : EJHG|July 24, 2019
Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genesMonika Morak, Kerstin Schaefer, Verena Steinke-Lange, et al.
Journal of Medical Genetics|December 16, 2021
Constitutional chromothripsis of the <i>APC</i> locus as a cause of genetic predisposition to colon cancerFlorentine Scharf, Rafaela Magalhaes Leal Silva, Monika Morak, et al.
Frontiers in Medicine|December 29, 2025
RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case seriesHannah Glonnegger, Doris Boeckelmann, Rebekka Wiedenhöfer, et al.
European Journal of Human Genetics : EJHG|June 8, 2022
Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working GroupMonika Morak, Marta Pineda, Alexandra Martins, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Cancer Biomarkers : Section a of Disease Markers|February 12, 2013
CD133 is a predictor of poor survival in head and neck squamous cell carcinomasMartin Canis, Axel Lechner, Brigitte Mack, et al.
European Journal of Pediatrics|September 19, 2009
A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosumUdo Koehler, Elke Holinski-Feder, Birgit Ertl-Wagner, et al.
Cytogenetic and Genome Research|December 10, 2023
Genome Mapping NomenclatureSarah Moore, Jean McGowan-Jordan, Adam C Smith, et al.
Genes|March 28, 2024
Optical Genome Mapping as a Potential Routine Clinical Diagnostic MethodHayk Barseghyan, Doris Eisenreich, Evgenia Lindt, et al.
Human Molecular Genetics|February 18, 2009
In vitro supplementation with dAMP/dGMP leads to partial restoration of mtDNA levels in mitochondrial depletion syndromesStefanie Bulst, Angela Abicht, Elke Holinski-Feder, et al.
Journal of Medical Genetics|June 30, 2011
Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndromeMonika Morak, Udo Koehler, Hans Konrad Schackert, et al.
European Journal of Human Genetics : EJHG|July 24, 2019
Full-length transcript amplification and sequencing as universal method to test mRNA integrity and biallelic expression in mismatch repair genesMonika Morak, Kerstin Schaefer, Verena Steinke-Lange, et al.
Journal of Medical Genetics|December 16, 2021
Constitutional chromothripsis of the <i>APC</i> locus as a cause of genetic predisposition to colon cancerFlorentine Scharf, Rafaela Magalhaes Leal Silva, Monika Morak, et al.
Frontiers in Medicine|December 29, 2025
RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case seriesHannah Glonnegger, Doris Boeckelmann, Rebekka Wiedenhöfer, et al.
European Journal of Human Genetics : EJHG|June 8, 2022
Splicing analyses for variants in MMR genes: best practice recommendations from the European Mismatch Repair Working GroupMonika Morak, Marta Pineda, Alexandra Martins, et al.
Pageof 3