Morten Hillmer
Ulm, BW, Germany
Last Updated: 09/26/2026
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Found 8 publications
Combined Heterozygous Genetic Variations in Complement C2 and C8B: An Explanation for Multidimensional Immune Imbalance?
Journal: Journal of innate immunity
Published: August 03, 2022
Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes.
Journal: Familial cancer
Published: May 04, 2022
Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial Cancer.
Journal: Cancer research
Published: November 17, 2021
Genetic Obesity in Children: Overview of Possible Diagnoses with a Focus on SH2B1 Deletion.
Journal: Hormone research in paediatrics
Published: June 29, 2021
Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome.
Journal: Genes, chromosomes & cancer
Published: November 30, 2018
Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identification.
Journal: Human mutation
Published: June 26, 2017
Fine mapping of meiotic NAHR-associated crossovers causing large NF1 deletions.
Journal: Human molecular genetics
Published: November 12, 2015
Identification of large NF1 duplications reciprocal to NAHR-mediated type-1 NF1 deletions.
Journal: Human mutation
Published: July 07, 2014
Showing 1-8 of 8
Last Updated: 09/26/2026