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10. Expanding the phenotype of hypomaturation amelogenesis imperfecta due to a novel SLC24A4 variant. Lepperdinger U; Maurer E; Witsch-Baumgartner M; Stigler R; Zschocke J; Lussi A; Kapferer-Seebacher I Clin Oral Investig; 2020 Oct; 24(10):3519-3525. PubMed ID: 32034543 [TBL] [Abstract][Full Text] [Related]
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17. Identification of the first multi-exonic WDR72 deletion in isolated amelogenesis imperfecta, and generation of a WDR72-specific copy number screening tool. Hentschel J; Tatun D; Parkhomchuk D; Kurth I; Schimmel B; Heinrich-Weltzien R; Bertzbach S; Peters H; Beetz C Gene; 2016 Sep; 590(1):1-4. PubMed ID: 27259663 [TBL] [Abstract][Full Text] [Related]
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