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Molecular Neurobiology
|
March 22, 2017
Cognitive Control Processes and Functional Cerebral Asymmetries: Association with Variation in the Handedness-Associated Gene LRRTM1
Christian Beste, Larissa Arning, Wanda M Gerding, et al.
Plos One
|
September 17, 2013
SOX9 duplication linked to intersex in deer
Regina Kropatsch, Gabriele Dekomien, Denis A Akkad, et al.
Brain Structure & Function
|
August 11, 2018
PLP1 and CNTN1 gene variation modulates the microstructure of human white matter in the corpus callosum
Catrona Anderson, Wanda M Gerding, Christoph Fraenz, et al.
Investigative Ophthalmology & Visual Science
|
January 1, 2016
Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families
Simone Kastner, Ina-Janine Thiemann, Gabriele Dekomien, et al.
Molecular Neurobiology
|
September 23, 2018
Myelin Water Fraction Imaging Reveals Hemispheric Asymmetries in Human White Matter That Are Associated with Genetic Variation in PLP1
Sebastian Ocklenburg, Catrona Anderson, Wanda M Gerding, et al.
International Journal of Cancer
|
January 22, 2022
Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patients
Wanda M Gerding, Marco Tembrink, Verena Nilius-Eliliwi, et al.
Human Molecular Genetics
|
June 18, 2011
Ccdc66 null mutation causes retinal degeneration and dysfunction
Wanda M Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, et al.
International Journal of Molecular Sciences
|
October 14, 2023
Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the <i>DMD</i> Gene
Leoni S Erbe, Sabine Hoffjan, Sören Janßen, et al.
International Journal of Molecular Sciences
|
October 16, 2024
Compound Heterozygous <i>RYR1</i> Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive <i>RYR1</i>-Related Myopathy
Sören Janßen, Leoni S Erbe, Moritz Kneifel, et al.
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Search research articles
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Showing results (21-30 of 29) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 29 results.
Molecular Neurobiology
|
March 22, 2017
Cognitive Control Processes and Functional Cerebral Asymmetries: Association with Variation in the Handedness-Associated Gene LRRTM1
Christian Beste, Larissa Arning, Wanda M Gerding, et al.
Plos One
|
September 17, 2013
SOX9 duplication linked to intersex in deer
Regina Kropatsch, Gabriele Dekomien, Denis A Akkad, et al.
Brain Structure & Function
|
August 11, 2018
PLP1 and CNTN1 gene variation modulates the microstructure of human white matter in the corpus callosum
Catrona Anderson, Wanda M Gerding, Christoph Fraenz, et al.
Investigative Ophthalmology & Visual Science
|
January 1, 2016
Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families
Simone Kastner, Ina-Janine Thiemann, Gabriele Dekomien, et al.
Molecular Neurobiology
|
September 23, 2018
Myelin Water Fraction Imaging Reveals Hemispheric Asymmetries in Human White Matter That Are Associated with Genetic Variation in PLP1
Sebastian Ocklenburg, Catrona Anderson, Wanda M Gerding, et al.
International Journal of Cancer
|
January 22, 2022
Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patients
Wanda M Gerding, Marco Tembrink, Verena Nilius-Eliliwi, et al.
Human Molecular Genetics
|
June 18, 2011
Ccdc66 null mutation causes retinal degeneration and dysfunction
Wanda M Gerding, Sabrina Schreiber, Tobias Schulte-Middelmann, et al.
International Journal of Molecular Sciences
|
October 14, 2023
Exome Sequencing and Optical Genome Mapping in Molecularly Unsolved Cases of Duchenne Muscular Dystrophy: Identification of a Causative X-Chromosomal Inversion Disrupting the <i>DMD</i> Gene
Leoni S Erbe, Sabine Hoffjan, Sören Janßen, et al.
International Journal of Molecular Sciences
|
October 16, 2024
Compound Heterozygous <i>RYR1</i> Variants in a Patient with Severe Congenital Myopathy: Case Report and Comparison with Additional Cases of Recessive <i>RYR1</i>-Related Myopathy
Sören Janßen, Leoni S Erbe, Moritz Kneifel, et al.
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of 3