Multiple Synostoses Syndrome Is Due to a Missense Mutation in Exon 2 of FGF9 Gene-Reference-Cited by-同舟云学术

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

Published:2009-07 Issue:1 Volume:85 Page:53-63
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Wu Xiao-lin,Gu Ming-min,Huang Lei,Liu Xue-song,Zhang Hong-xin,Ding Xiao-yi,Xu Jian-qiang,Cui Bin,Wang Long,Lu Shun-yuan,Chen Xiao-yi,Zhang Hai-guo,Huang Wei,Yuan Wen-tao,Yang Jiang-ming,Gu Qun,Fei Jian,Chen Zhu,Yuan Zhi-min,Wang Zhu-gang

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference48 articles.

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2. Somatic FGF9 mutations in colorectal and endometrial carcinomas associated with membranous beta-catenin;Abdel-Rahman;Hum. Mutat.,2008

3. Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis;Gong;Nat. Genet.,1999

4. GDF5 is a second locus for multiple-synostosis syndrome;Dawson;Am. J. Hum. Genet.,2006

5. The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4;Zimmerman;Cell,1996

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