1. Tooth agenesis and orofacial clefting: genetic brothers in arms?

   • M. Phan
   • F. Conte
   • C. E. L. Carels

   Review Open access 03 October 2016 Pages: 1299 - 1327

   

2. 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. Truong
   • L. D. Shriberg
   • J. R. Gruen

   Original Investigation Open access 17 August 2016 Pages: 1329 - 1341

   

3. Whole exome sequencing of Rett syndrome-like patients reveals the mutational diversity of the clinical phenotype

   • Mario Lucariello
   • Enrique Vidal
   • Manel Esteller

   Original Investigation Open access 19 August 2016 Pages: 1343 - 1354

   

4. Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways

   • Erin M. Hagen
   • Robert J. Sicko
   • James L. Mills

   Original Investigation 15 September 2016 Pages: 1355 - 1364

5. The disappearing San of southeastern Africa and their genetic affinities

   • Carina M. Schlebusch
   • Frans Prins
   • Himla Soodyall

   Original Investigation Open access 20 September 2016 Pages: 1365 - 1373

   

6. A mutation in ADIPOR1 causes nonsyndromic autosomal dominant retinitis pigmentosa

   • Jinlu Zhang
   • Changguan Wang
   • Liping Yang

   Original Investigation 21 September 2016 Pages: 1375 - 1387

   

7. Associations of cytochrome P450 oxidoreductase genetic polymorphisms with smoking cessation in a Chinese population

   • Huijie Li
   • Suyun Li
   • Chongqi Jia

   Original Investigation 22 September 2016 Pages: 1389 - 1397

   

8. De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease

   • Lijiang Ma
   • Yavuz Bayram
   • Wendy K. Chung

   Original Investigation 28 September 2016 Pages: 1399 - 1409