-
HipSci___Whole_Exome_sequencing___Alport
Study
EGAS00001001974
-
HipSci HumanHT 12 Expression BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002030
-
Familial_Thrombocytosis_germline_exome_sequencing
Study
EGAS00001000088
-
HipSci___Whole_Exome_sequencing___Retinitis_Pigmentosa
Study
EGAS00001001984
-
HipSci Illumina 450K Methylation analysis-Rare_BBS
Study
EGAS00001001274
-
HipSci___Whole_Exome_sequencing___BPD
Study
EGAS00001001976
-
HipSci HumanExome BeadChip analysis - Alport Syndrome
Study
EGAS00001002009
-
HipSci HumanExome BeadChip analysis - Retinitis Pigmentosa
Study
EGAS00001002015
-
HipSci HumanHT 12 Expression BeadChip analysis - Kabuki syndrome
Study
EGAS00001002022
-
HipSci HumanHT 12 Expression BeadChip analysis - Congenital Hyperinsulinia
Study
EGAS00001002025