Associated Papers
Functional Validation of Noncoding Variants Associated With Nonsyndromic Orofacial Cleft.
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Human Mutation, 2025
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Supplement: 6824122.f3.xlsx › Table_S3
Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia.
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Frontiers in Genetics, 2021
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Supplement: Table_1.XLSX › Supplementary_table_1
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