Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism-Reference-Cited by-同舟云学术

Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism

Published:2019-05 Issue: Volume:122 Page:193-198
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Kajii Takashi S.,Oka Akira,Saito Fumio,Mitsui Jun,Iida Junichiro

Funder

MEXT

JSPS

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

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4. Genes, genetics, and Class III malocclusion;Xue;Orthod. Craniofac. Res.,2010

5. Genetics of the dentofacial variation in human malocclusion;Moreno Uribe;Orthod. Craniofac. Res.,2015

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