Literature DB >> 5257851

[An unusual case of hereditary developmental anomalies of the cuspids and molars].

J Dénes, A Csiba.   

Abstract

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Mesh：

Year:  1969        PMID： 5257851

Source DB:  PubMed          Journal:  Fogorv Sz        ISSN： 0015-5314


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  4 in total

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Authors:  Agnès Bloch-Zupan; Jane R Goodman
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2.  Chromosome 11q13 deletion syndrome.

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3.  Clinical, pathological, and genetic evaluations of Chinese patient with otodental syndrome and multiple complex odontoma: Case report.

Authors:  Anqi Liu; Meiling Wu; Xiaohe Guo; Hao Guo; Zhifei Zhou; Kewen Wei; Kun Xuan
Journal:  Medicine (Baltimore)       Date:  2017-02       Impact factor: 1.889

4.  Three years of follow-up of otodental syndrome in 3-year-old Chinese boy: a rare case report.

Authors:  Ji-Mei Su; Su-Juan Zeng; Xiao-Wei Ye; Zhi-Fang Wu; Xin-Wen Huang; Janak L Pathak
Journal:  BMC Oral Health       Date:  2019-07-25       Impact factor: 2.757
  4 in total

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