26t
2a
aberrations
anemia
blackfan
cgh
congenital
copy
dba
deletions
diamond
fourfold
haploinsufficiency
heterozygous
hyperactivation
hypoproliferative
korean
malformations
predisposition
reductions
rpl11
rpl35a
rpl5
rps10
rps17
rps19
rps24
supports
variations
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