APA
Kanca O., Andrews J. C., Lee P., Patel C., Braddock S. R., Slavotinek A. M., Cohen J. S., Gubbels C. S., Aldinger K. A., Williams J., Indaram M., Fatemi A., Yu T. W., Agrawal P. B., Vezina G., Simons C., Crawford J., Lau C. C., Chung W. K., Markello T. C., Dobyns W. B., Adams D. R., Gahl W. A., Wangler M. F., Yamamoto S., Bellen H. J. & Malicdan M. C. V. (2019). De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. : American journal of human genetics.
Chicago
Kanca Oguz, Andrews Jonathan C, Lee Pei-Tseng, Patel Chirag, Braddock Stephen R, Slavotinek Anne M, Cohen Julie S, Gubbels Cynthia S, Aldinger Kimberly A, Williams Judy, Indaram Maanasa, Fatemi Ali, Yu Timothy W, Agrawal Pankaj B, Vezina Gilbert, Simons Cas, Crawford Joanna, Lau C Christopher, Chung Wendy K, Markello Thomas C, Dobyns William B, Adams David R, Gahl William A, Wangler Michael F, Yamamoto Shinya, Bellen Hugo J and Malicdan May Christine V. 2019. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. : American journal of human genetics.
Harvard
Kanca O., Andrews J. C., Lee P., Patel C., Braddock S. R., Slavotinek A. M., Cohen J. S., Gubbels C. S., Aldinger K. A., Williams J., Indaram M., Fatemi A., Yu T. W., Agrawal P. B., Vezina G., Simons C., Crawford J., Lau C. C., Chung W. K., Markello T. C., Dobyns W. B., Adams D. R., Gahl W. A., Wangler M. F., Yamamoto S., Bellen H. J. and Malicdan M. C. V. (2019). De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. : American journal of human genetics.
MLA
Kanca Oguz, Andrews Jonathan C, Lee Pei-Tseng, Patel Chirag, Braddock Stephen R, Slavotinek Anne M, Cohen Julie S, Gubbels Cynthia S, Aldinger Kimberly A, Williams Judy, Indaram Maanasa, Fatemi Ali, Yu Timothy W, Agrawal Pankaj B, Vezina Gilbert, Simons Cas, Crawford Joanna, Lau C Christopher, Chung Wendy K, Markello Thomas C, Dobyns William B, Adams David R, Gahl William A, Wangler Michael F, Yamamoto Shinya, Bellen Hugo J and Malicdan May Christine V. De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. : American journal of human genetics. 2019.