Tooth agenesis and orofacial clefting: genetic brothers in arms? M. PhanF. ConteC. E. L. Carels Review Open access 03 October 2016 Pages: 1299 - 1327
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disorders D. T. TruongL. D. ShribergJ. R. Gruen Original Investigation Open access 17 August 2016 Pages: 1329 - 1341
Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype Mario LucarielloEnrique VidalManel Esteller Original Investigation Open access 19 August 2016 Pages: 1343 - 1354
Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways Erin M. HagenRobert J. SickoJames L. Mills Original Investigation 15 September 2016 Pages: 1355 - 1364
The disappearing San of southeastern Africa and their genetic affinities Carina M. SchlebuschFrans PrinsHimla Soodyall Original Investigation Open access 20 September 2016 Pages: 1365 - 1373
A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa Jinlu ZhangChangguan WangLiping Yang Original Investigation 21 September 2016 Pages: 1375 - 1387
Associations of cytochrome P450 oxidoreductase genetic polymorphisms with smoking cessation in a Chinese population Huijie LiSuyun LiChongqi Jia Original Investigation 22 September 2016 Pages: 1389 - 1397
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease Lijiang MaYavuz BayramWendy K. Chung Original Investigation 28 September 2016 Pages: 1399 - 1409