Functional Analysis of RUNX2 Mutations in Japanese Patients with Cleidocranial Dysplasia Demonstrates Novel Genotype-Phenotype Correlations - Concepedia

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Functional Analysis of RUNX2 Mutations in Japanese Patients with Cleidocranial Dysplasia Demonstrates Novel Genotype-Phenotype Correlations

DOI Full Paper Access

159

Citations

59

References

2002

Year

Taketoshi Yoshida, Hirokazu Kanegane, Motomi Osato, Masatoshi Yanagida, Toshio Miyawaki, Yoshiaki Ito, Katsuya Shigesada

The American Journal of Human Genetics

Genetic DisorderGeneticsNeurologyDisease Gene IdentificationFunctional AnalysisRunx2 MutationsMedicineJapanese PatientsClinical Genetics

References

	Year	Citations

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