Testing reported associations of genetic risk factors for oral clefts in a large Irish study population

BACKGROUND: Suggestive, but not conclusive, studies implicate many genetic variants in oral cleft etiology. We used a large, ethnically homogenous study population to test whether reported associations between nonsyndromic oral clefts and 12 genes (CLPTM1, CRISPLD2, FGFR2, GABRB3, GLI2, IRF6, PTCH1,...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Carter, Tonia C., Molloy, Anne M., Pangilinan, Faith, Troendle, James F., Kirke, Peadar N., Conley, Mary R., Orr, David J. A., Earley, Michael, McKiernan, Eamon, Lynn, Ena C., Doyle, Anne, Scott, John M., Brody, Lawrence C., Mills, James L.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2010
Témata:
Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3503531/
https://ncbi.nlm.nih.gov/pubmed/19937600
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.20639
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky