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[Analysis of clinical phenotype and genetic variant in a Chinese pedigree affected with cleidocranial dysplasia]
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Genotype‐phenotype analysis of selective failure of tooth eruption—A systematic review
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Newborn with isolated severe deficiency of cranial vault ossification: a case of cleidocranial dysplasia
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Osteo-/Odontogenic Differentiation of Induced Mesenchymal Stem Cells Generated through Epithelial–Mesenchyme Transition of Cultured Human Keratinocytes
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Computational Modeling of TP63–TP53 Interaction and Rational Design of Inhibitors: Implications for Therapeutics
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TP63 Gene Mutations in Chinese P63 Syndrome Patients
11天前
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