Sort   by:  
 Page size 
UnknownA Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and Deafness.
Not available
S-EPMC8970462 | biostudies-literature
UnknownGenetics of membranous nephropathy.
Not available
S-EPMC6113634 | biostudies-literature
UnknownGenetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome.
Not available
S-EPMC6683715 | biostudies-literature
UnknownGenetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies.
Not available
S-EPMC5837679 | biostudies-literature
GenomicsUC
WTCCC2 project Ulcerative Colitis (UC) samples
EGAD00000000025 | EGA
GenomicsWTCCC2 case-control study for Ulcerative Colitis
WTCCC2 project genome-wide case-control association study for Ulcerative Colitis (UC) using the 1958 British Birth Cohort and the UK National Blood Service collections as controls.
EGAS00000000084 | EGA
GenomicsWTCCC2 project controls - 1958 British Birth Cohort and National Blood Service
WTCCC2 project controls - 1958 British Birth Cohort and National Blood Service
EGAS00000000028 | EGA
GenomicsATD
WTCCC1 project Autoimmune Thyroid Disease (ATD) samples
EGAD00000000011 | EGA
GenomicsBC
WTCCC1 project Breast cancer (BC) samples
EGAD00000000013 | EGA
GenomicsMS
WTCCC1 project Multiple Sclerosis (MS) samples
EGAD00000000012 | EGA
Sort   by:  
 Page size