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Human enamel phenotype associated with amelogenesis imperfecta and a kallikrein-4 (g.2142G>A) proteinase mutation

✍ Scribed by J. Tim Wright; Bill Daly; Darrin Simmons; Sung Hong; Suzanne P. Hart; Tom C. Hart; Phimon Atsawasuwan; Mitsuo Yamauchi


Book ID
111256669
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
242 KB
Volume
114
Category
Article
ISSN
0909-8836

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