Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene - Concepedia

Concepedia

Publication | Open Access

Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene

DOI Full Paper Access

85

Citations

41

References

2009

Year

Xiaolin Wu, Ming-min Gu, Lei Huang, Xuesong Liu, Hongxin Zhang, Xiaoyi Ding, Jianqiang Xu, Bin Cui, Long Wang, Shunyuan Lu,

The American Journal of Human Genetics

Mendelian DisorderMultiple Synostoses SyndromeFgf9 GeneConnective Tissue DiseaseGenetic DisorderGeneticsClinical GeneticsPathologyMolecular GeneticsDisease Gene IdentificationMedicineMonogenic DisordersExon 2

References

	Year	Citations

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