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IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
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Association of Age at Diagnosis and Genetic Mutations in Patients with Neuroblastoma
Study
EGAS00001000213
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Exome-sequencing identifies new oncogenes and tumor suppressor genes recurrently altered in hepatocellular carcinoma
Study
EGAS00001000217
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UK10K NEURO GURLING
Study
EGAS00001000225
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Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells
Study
EGAS00001000231
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Molecular analysis of giant cell lesions
Study
EGAS00001002910
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
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HipSci-Whole Exome sequencing-healthy volunteers
Study
EGAS00001000592
-
Chromatin 3D interactions mediate genetic effects on gene expression
Study
EGAS00001003485