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Clinical and genetic analysis of a rare syndrome associated with neoteny
Study
EGAS00001002419
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The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
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Whole exome sequencing in patients with ALS and concomitant FTD lacking the C9orf72 repeat expansion
Study
EGAS00001002439
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Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Study
EGAS00001002440
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Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia
Study
EGAS00001005075
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Comprehensive Molecular Analysis of Colon Cancer for the Identification and Validation of New Biomarkers
Study
EGAS00001002453
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The demographic history and mutational load of African hunter-gatherers and farmers
Study
EGAS00001002457
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ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
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Genomic and epigenomic characterization of juvenile myelomonocytic leukemia (JMML)
Study
EGAS00001002511
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Sampling of multi-centric lower grade glioma influences management and provides insight into gliomagenesis
Study
EGAS00001002495