1. Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate

   • Elizabeth J. Leslie
   • Jenna C. Carlson
   • Mary L. Marazita

   Original Investigation 04 January 2017 Pages: 275 - 286

   

2. Association of AHSG with alopecia and mental retardation (APMR) syndrome

   • M. Reza Sailani
   • Fereshteh Jahanbani
   • Michael P. Snyder

   Original Investigation 04 January 2017 Pages: 287 - 296

   

3. Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype

   • Nuria C. Bramswig
   • O. Caluseriu
   • D. Wieczorek

   Original Investigation 25 January 2017 Pages: 297 - 305

   

4. Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes

   • Ilaria Parenti
   • María E. Teresa-Rodrigo
   • Frank J. Kaiser

   Original Investigation 24 January 2017 Pages: 307 - 320

   

5. Novel FAM134B mutations and their clinicopathological significance in colorectal cancer

   • Farhadul Islam
   • Vinod Gopalan
   • Alfred K.-Y. Lam

   Original Investigation 31 January 2017 Pages: 321 - 337

   

6. Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies

   • Maja Hempel
   • Teresa Casar Tena
   • Davor Lessel

   Original Investigation 08 February 2017 Pages: 339 - 346

   

7. Erratum to: IL8 gene as modifier of cystic fibrosis: unraveling the factors which influence clinical variability

   • Larissa Lazzarini Furlan
   • Fernando Augusto Lima Marson
   • Dorotéia Rossi Silva Souza

   Erratum 03 February 2017 Pages: 347 - 348