MSX1 Gene is Deleted in Wolf-Hirschhorn Syndrome Patients with Oligodontia
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概要
- 論文の詳細を見る
- 2003-12-01
著者
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Nieminen P.
Department Of Pedodontics And Orthodontics Institute Of Dentistry
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Nieminen P.
Institute Of Dentistry And Institute Of Biotechnology University Of Helsinki
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Knuutila S.
Department Of Medical Genetics Haartman Institute Helsinki University Central Hospital University Of
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Thesleff I.
Institute Of Biotechnology University Of Helsinki
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KOTILAINEN J.
Institute of Dentistry, Biomedicum, PO Box 63, FIN-00014 University of Helsinki
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AALTO Y.
Department of Medical Genetics, Haartman Institute, Helsinki University Central Hospital, University
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PIRINEN S.
Institute of Dentistry, Biomedicum, PO Box 63, FIN-00014 University of Helsinki
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Aalto Y.
Department Of Medical Genetics Haartman Institute Helsinki University Central Hospital University Of
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Aalto Y.
Department Of Medical Genetics Haartman Institute And Helsinki University Central Hospital Universit
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Pirinen S.
Department Of Pedodontics And Orthodontics Institute Of Dentistry
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Kotilainen J.
Institute Of Dentistry Biomedicum Po Box 63 Fin-00014 University Of Helsinki
関連論文
- Novel Mutation of the Initiation Codon of PAX9 Causes Oligodontia
- Laminin γ2 Expression is Developmentally Regulated during Murine Tooth Morphogenesis and is Intense in Ameloblasts
- The Epithelium-Tooth Interface : A Basal Lamina Rich in Laminin-5 and Lacking Other Known Laminin Isoforms
- MSX1 Gene is Deleted in Wolf-Hirschhorn Syndrome Patients with Oligodontia
- Characteristics of Incisor-Premolar Hypodontia in Families
- Gene Defect in Hypodontia : Exclusion of EGF, EGFR, and FGF-3 as Candidate Genes
- Gene Expression Profiling of Ameloblastoma and Human Tooth Germ by Means of a cDNA Microarray
- Palatal Displacement of Canine is Genetic and Related to Congenital Absence of Teeth