Associated Papers
Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.
He Q et al.
Advanced Science (weinheim, Baden-wurttemberg, Germany), 2025
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Supplement: ADVS-12-e12073-s004.xlsx › Sheet1
Mutations in HFM1 in recessive primary ovarian insufficiency.
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Supplement: nejmc1310150_appendix.pdf
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