Associated Papers
Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability.
Popp B et al.
Bmc Cancer, 2019
Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract.
Li J et al.
Orphanet Journal of Rare Diseases, 2018
29914532 (PubMed )
Supplement: 13023_2018_828_MOESM4_ESM.xls › Sheet1
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