Associated Papers
Novel NOG (p.P42S) mutation causes proximal symphalangism in a four-generation Chinese family.
Sha Y et al.
Bmc Medical Genetics, 2019
31370824 (PubMed )
Supplement: 12881_2019_864_MOESM2_ESM.xlsx › Sheet1
Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa.
Arno G et al.
American Journal of Human Genetics, 2016
27889058 (PubMed )
Supplement: mmc1.pdf
Germline mutations in MAP3K6 are associated with familial gastric cancer.
Gaston D et al.
Plos Genetics, 2014
25340522 (PubMed )
Supplement: pgen.1004669.s004.xlsx › Sheet1
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