Kevin A Strauss

Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.

Peter B Crino, David A Ramsay, David W Craig, 2007, Brain : a journal of neurology.

A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder

Kristian Cibulskis, Carrie Sougnez, Stacey Gabriel, 2012, Human mutation.

One community's effort to control genetic disease.

E. Puffenberger, K. Strauss, D. Morton, 2012, American journal of public health.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.