Intra-familial tests of association between Familial Idiopathic Scoliosis and markers on 9q31.3-q34.3 and 16p12.3-q22.2

OBJECTIVE: Custom genotyping of markers in families with Familial Idiopathic Scoliosis (FIS) were used to fine-map candidate regions on chromosomes 9 and 16 in order to identify candidate genes that contribute to this disorder and prioritize them for next generation sequence analysis. METHODS: Candi...

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Autores principales: Miller, Nancy H., Justice, Cristina M., Marosy, Beth, Swindle, Kandice, Kim, Yoonhee, Roy-Gagnon, Marie-Hélène, Sung, Heejong, Behneman, Dana, Doheny, Kimberly F., Pugh, Elizabeth, Wilson, Alexander F.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2012
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4123546/
https://ncbi.nlm.nih.gov/pubmed/23154503
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000343751
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