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Structural variants disrupt a critical regulatory region downstream of FOXG1
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Advances in CRISPR-mediated knock-in of disease-related variants in zebrafish
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Understanding human linkeropathies : study of the phenotypic and molecular consequences of defective biosynthesis of the glycosaminoglycan tetrasaccharide linker region
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Evaluation of a novel antisense oligonucleotide therapy targeting a 5’UTR mutation in the RDH12 gene
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- Conference Paper
- C3
- open access
Towards improved Parsortix® efficiency for circulating tumor cell enrichment in pancreatic cancer
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- Conference Paper
- C3
- open access
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder