## Abstract ## Objectives/Hypothesis: Interferon regulatory factor 6 (__IRF6__), the gene that causes van der Woude syndrome (VWS), is a candidate gene for nonsyndromic cleft lip with or without cleft palate (NSCLP) because a number of studies have supported an association between NSCLP and single
✦ LIBER ✦
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population
✍ Scribed by Luciano A. Brito; Camila F.S. Bassi; Cibele Masotti; Carolina Malcher; Kátia M. Rocha; David Schlesinger; Daniela F. Bueno; Lucas A. Cruz; Ligia K. Barbara; Débora R. Bertola; Diogo Meyer; Diogo Franco; Nivaldo Alonso; Maria Rita Passos-Bueno
- Book ID
- 115549367
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 138 KB
- Volume
- 158A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The association between interferon regul
✍
Gillian R. Diercks; Tom T. Karnezis; David T. Kent; Carlos Flores; Gloria H. Su;
📂
Article
📅
2009
🏛
John Wiley and Sons
🌐
English
⚖ 113 KB
Linkage disequilibrium between IRF6 vari
✍
José Suazo; José Luis Santos; Lilian Jara; Rafael Blanco
📂
Article
📅
2008
🏛
John Wiley and Sons
🌐
English
⚖ 53 KB
👁 2 views
Interferon regulatory factor (IRF)-6 820
✍
Hyun Soo Park; Kun Woo Kim; Cha-Hui Lee; Soon-Sup Shim; Joong Shin Park; Jong Kw
📂
Article
📅
2006
🏛
Elsevier Science
🌐
English
⚖ 58 KB
Risk variants inBMP4promoters for nonsyn
✍
José Suazo; Julio C Tapia; José Luis Santos; Víctor G Castro; Alicia Colombo; Ra
📂
Article
📅
2011
🏛
BioMed Central
🌐
English
⚖ 501 KB
Contribution of variants in and near the
✍
Iman Salahshourifar; Wan Azman Wan Sulaiman; Bin Alwi Zilfalil; Ahmad Sukari Hal
📂
Article
📅
2011
🏛
John Wiley and Sons
🌐
English
⚖ 249 KB
👁 2 views
Genetic risk factors for nonsyndromic cl
✍
Augusto Rojas-Martinez; Heiko Reutter; Oscar Chacon-Camacho; Rafael B. R. Leon-C
📂
Article
📅
2010
🏛
John Wiley and Sons
🌐
English
⚖ 68 KB
👁 2 views
## Abstract **INTRODUCTION:** Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common of all birth defects. NSCL/P has a multifactorial etiology that includes both genetic and environmental factors. The __IRF6__ gene and three further susceptibility loci at 8q24, 10q2