Using whole-exome sequencing to identify inherited causes of autism. uri icon

authors

  • Yu, Timothy W
  • Malik, Athar N
  • D'Gama, Alissa M
  • Elaine Lim, PhD
  • Sanders, Stephan J
  • Mochida, Ganesh H
  • Partlow, Jennifer N
  • Sunu, Christine M
  • Felie, Jillian M
  • Rodriguez, Jacqueline
  • Nasir, Ramzi H
  • Chahrour, Maria H
  • Ware, Janice
  • Joseph, Robert M
  • Hill, R Sean
  • Kwan, Benjamin Y
  • Al-Saffar, Muna
  • Mukaddes, Nahit M
  • Hashmi, Asif
  • Balkhy, Soher
  • Gascon, Generoso G
  • Hisama, Fuki M
  • Coulter, Michael E
  • LeClair, Elaine
  • Poduri, Annapurna
  • Oner, Ozgur
  • Al-Saad, Samira
  • Al-Awadi, Sadika A
  • Bastaki, Laila
  • Ben-Omran, Tawfeg
  • Teebi, Ahmad S
  • Al-Gazali, Lihadh
  • Eapen, Valsamma
  • Jiralerspong, Sarn
  • Stevens, Christine R
  • Rappaport, Leonard
  • Gabriel, Stacey B
  • Markianos, Kyriacos
  • State, Matthew W
  • Greenberg, Michael E
  • Taniguchi, Hisaaki
  • Braverman, Nancy E
  • Morrow, Eric M
  • Walsh, Christopher A
  • Okamura-Ikeda, Kazuko
  • Ataman, Bulent
  • Schmitz-Abe, Klaus
  • Harmin, David A
  • Adli, Mazhar

publication date

  • January 1, 2013

published in