2010 list of SureSelect publications:
- Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing. Lalonde E et al. Hum Mutat. 2010 31, p918-23.
- Terminal Osseous Dysplasia Is Caused by a Single Recurrent Mutation in the FLNA Gene. Sun et al. Am J Hum Genet. (2010) 9, p146-153.
- Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing. Walsh et al. PNAS (2010) online release
- Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82. Walsh et al. Am J Hum Genet. (2010) online release
- De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Hoischen A et al. Nat Genet. (2010) 42, p483-5.
- Massively parallel sequencing of exons on the X chromosome identifies RBM10 as the gene that causes a syndromic form of cleft palate. Johnston JJ et al. Am J Hum Genet. (2010) 14, p743-8
- F6 mutations in T-cell acute lymphoblastic leukemia. Van Vlierberghe P, et al. Nat Genet. (2010) 42, p338-42