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Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome wide association on chromosome 1p22

BACKGROUND: Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is a common birth defect with complex etiology reflecting the action of multiple genetic and/or environmental factors. Genome wide association studies have successfully identified five novel loci associated with NSCL/P includin...

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Detalhes bibliográficos
Main Authors: Leslie, Elizabeth J, Mansilla, M Adela, Biggs, Leah C, Schuette, Kristi, Bullard, Steve, Cooper, Margaret, Dunnwald, Martine, Lidral, Andrew C, Marazita, Mary L, Beaty, Terri H, Murray, Jeffrey C
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3501616/
https://ncbi.nlm.nih.gov/pubmed/23008150
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.23076
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