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Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
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Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
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Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
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A rare CTSC mutation in Papillon-Lefèvre Syndrome
Study
EGAS00001005040
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SudanMitoSeq: Sudanese mitochondrial sequencing
Study
EGAS00001005669
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Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
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Exome sequencing reveals pathogenic variants in known and novel candidate genes for severe sperm motility disorders
Study
EGAS00001005018
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Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
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Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs
Study
EGAS00001005444
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MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__head___neck
Study
EGAS00001005450