Cystic Fibrosis Transmembrane Regulator Gene (CFTR) is Associated with Abnormal Enamel Formation
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概要
- 論文の詳細を見る
- 2002-07-01
著者
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Wright J.
Department Of Pediatric Dentistry School Of Dentistry University Of North Carolina
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Wright J.
Department Of Pediatric Dentistry Cb# 7450 School Of Dentistry University Of North Carolina At Chape
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Wright J.
Department Of Pediatric Dentistry School Of Dentistry The University Of North Carolina At Chapel Hil
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ARQUITT C.
Private Practice, Pediatric Dentistry
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BOYD C.
Department of Pediatric Dentistry, School of Dentistry, The University of North Carolina at Chapel H
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Arquitt C.
Private Practice Pediatric Dentistry
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Boyd C.
Department Of Pediatric Dentistry School Of Dentistry University Of North Carolina
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Boyd C.
Department Of Pediatric Dentistry School Of Dentistry The University Of North Carolina At Chapel Hil
関連論文
- Protein Characterization of Fluorosed Human Enamel
- Cystic Fibrosis Transmembrane Regulator Gene (CFTR) is Associated with Abnormal Enamel Formation
- The Amelogenin C-Terminus Is Required for Enamel Development
- Abnormal Enamel Development in a Cystic Fibrosis Transgenic Mouse Model
- Unique Enamel Phenotype Associated with Amelogenin Gene (AMELX) Codon 41 Point Mutation
- Altered pH Regulation During Enamel Development in the Cystic Fibrosis Mouse Incisor
- Defining the Contribution of Genetics in the Etiology of Dental Caries
- Microgenomics of Ameloblastoma