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The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome
Study
EGAS00000000129
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DO NOT USE - Whole genome sequencing of SI-NETs from five patients
Study
EGAS00001004435
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Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
Study
EGAS00000000097
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Department of Human Genetics, Radboud University Nijmegen Medical Centre, Data Access Committee
Dac
EGAC00001000076
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Frequent mutation of the major cartilage collagen gene, COL2A1, in chondrosarcoma
Dataset
EGAD00001000358
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13K T2D-GENES analysis files
Dataset
EGAD00010001188
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Counts: Brain transcriptome of hereditary cerebral haemorrhage with amyloidosis–Dutch type (HCHWA-D)
Dataset
EGAD00010001457
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UK_RCC_GWAS
Dataset
EGAD00010002310
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GSA QCed data
Dataset
EGAD00010002568
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ONGOING CHROMOSOMAL INSTABILITY ACROSS ANEUPLOID SUBTYPES OF CHILDHOOD B-CELL ACUTE LYMPHOBLASTIC LEUKEMIA ASSOCIATES WITH DISEASE PROGRESSION
Dataset
EGAD50000000029