A Survey of Next-Generation–Sequencing Technologies - Next Generation Sequencing Technologies in Medical Genetics - page 22

Volpi L, Roversi G, Colombo EA et al (2010) Targeted next-generation sequencing appoints
c16orf57 as clericuzio-type poikiloderma with neutropenia gene. Am J Hum Genet 86:72-76.
doi: 10.1016/j.ajhg.2009.11.014
Walsh T, Shahin H, Elkan-Miller T et al (2010) Whole exome sequencing and homozygosity map-
ping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hear-
ing loss DFNB82. Am J Hum Genet 87:90-94. doi: 10.1016/j.ajhg.2010.05.010
Wheeler DA, Srinivasan M, Egholm M et al (2008) The complete genome of an individual by mas-
sively parallel DNA sequencing. Nature 452:872-876. doi: 10.1038/nature06884
Zheng J, Miller KK, Yang T et al (2011) Carcinoembryonic antigen-related cell adhesion molecule
16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).
Proc Natl Acad Sci U S A 108:4218-4223. doi: 10.1073/pnas.1005842108