Elizabeth C Engle

Human disorders of axon guidance

E. Engle, Alicia A Nugent, Adrianne L Kolpak, 2012, Current Opinion in Neurobiology.

Magnetic resonance imaging evidence for widespread orbital dysinnervation in congenital fibrosis of extraocular muscles due to mutations in KIF21A.

Joseph L Demer, J. Demer, R. Clark, 2005, Investigative ophthalmology & visual science.

Human genetic disorders of axon guidance.

E. Engle, Elizabeth C Engle, 2010, Cold Spring Harbor perspectives in biology.

Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders

Yiping Shen, Sandra Friedman, Bai-Lin Wu, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Human CHN1 Mutations Hyperactivate α2-Chimaerin and Cause Duane's Retraction Syndrome

Alfonso Baldi, Michelle Cheung, Mustafa Sahin, 2008, Science.

Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports

Yiping Shen, Va Lip, Catherine A Brownstein, 2016, American journal of medical genetics. Part A.

Genetic basis of congenital strabismus.

E. Engle, Elizabeth C Engle, 2007, Archives of ophthalmology.