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Identification of the cause of juvenile parkinsonism in a case_SYNJ1
Study
EGAS00001007686
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Prevalence and association of microsatellite instability and Lynch syndrome Pan-Cancer and development of a personalized cancer risk prediction tool for Lynch syndrome carriers in India
Study
EGAS50000001449
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A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi
Study
EGAS00001002075
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The Intestinal Bacterial Metagenome in Pediatric Non-Alcoholic Fatty Liver Disease (NAFLD)
Study
phs001837
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Whole-exome sequencing identifies new pathogenic germline variants in patients with colorectal polyposis
Study
EGAS50000000591
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'IL-17A-Producing ILC3s and Duodenal Adenoma in FAP'
Study
EGAS00001007347
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Sample Multiplexing Oligo Comparison
Study
EGAS50000000153
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Renal_Follow_Up_Series
Study
EGAS00001000095
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Somatic_mutation_and_clonal_evolution_in_the_human_bladder_Novaseq
Study
EGAS00001003433
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Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma
Dataset
EGAD00001000134