Katja Kloth-Stachnau - JoVE Visualize

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Clinical Genetics|January 13, 2026

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype CorrelationAnastasia Maria Licata, Elke Botzenhart, Katja Kloth-Stachnau, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2026

Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omicsUgo Sorrentino, Melanie Brugger, Alice Saparov, et al.

Acta Neuropathologica|December 2, 2022

Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohortsMartin Mynarek, Denise Obrecht, Martin Sill, et al.

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Showing results (1-10 of 3) with videos related to

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Clinical Genetics|January 13, 2026

Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype-Phenotype CorrelationAnastasia Maria Licata, Elke Botzenhart, Katja Kloth-Stachnau, et al.

Movement Disorders : Official Journal of the Movement Disorder Society|July 9, 2026

Resolving Complex Structural Variants in Undiagnosed Rare Movement Disorders via Multimodal Genomics and Multi-omicsUgo Sorrentino, Melanie Brugger, Alice Saparov, et al.

Acta Neuropathologica|December 2, 2022

Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohortsMartin Mynarek, Denise Obrecht, Martin Sill, et al.

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