Search Results - Kantaputra, P.N.

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  1. 1
    GREMLIN 2 Mutations and Dental Anomalies

    GREMLIN 2 Mutations and Dental Anomalies by Kantaputra, P.N., Kaewgahya, M., Hatsadaloi, A., Vogel, P., Kawasaki, K., Ohazama, A., Ketudat Cairns, J.R.

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    Heterozygous Mutation in the SAM Domain of p63 Underlies Rapp-Hodgkin Ectodermal Dysplasia

    Heterozygous Mutation in the SAM Domain of p63 Underlies Rapp-Hodgkin Ectodermal Dysplasia by Kantaputra, P.N., Hamada, T., Kumchai, T., McGrath, J.A.

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  3. 3
    WNT10B mutations associated with isolated dental anomalies

    WNT10B mutations associated with isolated dental anomalies by Kantaputra, P.N., Hutsadaloi, A., Kaewgahya, M., Intachai, W., German, R., Koparal, M., Leethanakul, C., Tolun, A., Ketudat Cairns, J.R.

    Published in Clinical genetics
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    Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations

    Cleft Lip with Cleft Palate, Ankyloglossia, and Hypodontia are Associated with TBX22 Mutations by Kantaputra, P.N., Paramee, M., Kaewkhampa, A., Hoshino, A., Lees, M., McEntagart, M., Masrour, N., Moore, G.E., Pauws, E., Stanier, P.

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