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Your search keyword '"van Roosmalen, Markus J."' showing total 13 results

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13 results on '"van Roosmalen, Markus J."'

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1. Mitochondrial H2O2 release does not directly cause damage to chromosomal DNA

3. Reconstructing single-cell karyotype alterations in colorectal cancer identifies punctuated and gradual diversification patterns

4. Optimizing Nanopore sequencing-based detection of structural variants enables individualized circulating tumor DNA-based disease monitoring in cancer patients

5. Partner independent fusion gene detection by multiplexed CRISPR-Cas9 enrichment and long read nanopore sequencing

6. Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants

7. An organoid platform for ovarian cancer captures intra- and interpatient heterogeneity

8. Identification of human D lactate dehydrogenase deficiency

9. Mapping and phasing of structural variation in patient genomes using nanopore sequencing

10. Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells

11. The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

12. Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations

13. Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

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