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Author/Creator Engle, Elizabeth C

2. Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometry. Issue 1 (14th February 2020)

Authors:
Sadeghi, Neda; Hutchinson, Elizabeth; Van Ryzin, Carol; FitzGibbon, Edmond J; Butman, John A; Webb, Bryn D; Facio, Flavia; Brooks, Brian P; Collins, Francis S; Jabs, Ethylin Wang; Engle, Elizabeth C; Manoli, Irini; Pierpaoli, Carlo
Journal:
Brain communications
Issue:
Volume 2:Issue 1(2020)
Page Start:
Record Type:
Journal Article
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3. Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant. Issue 4 (13th July 2019)

Authors:
Thomas, Mervyn G; Maconachie, Gail D E; Constantinescu, Cris S; Chan, Wai-Man; Barry, Brenda; Hisaund, Michael; Sheth, Viral; Kuht, Helen J; Dineen, Rob A; Harieaswar, Sreemathi; Engle, Elizabeth C; Gottlob, Irene
Journal:
British journal of ophthalmology
Issue:
Volume 104:Issue 4(2020)
Page Start:
547
Record Type:
Journal Article
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4. Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humans. (18th June 2019)

Authors:
Whitman, Mary C; Miyake, Noriko; Nguyen, Elaine H; Bell, Jessica L; Matos Ruiz, Paola M; Chan, Wai-Man; Di Gioia, Silvio Alessandro; Mukherjee, Nisha; Barry, Brenda J; Bosley, T M; Khan, Arif O; Engle, Elizabeth C
Journal:
Human molecular genetics
Issue:
Volume 28:Number 18(2019)
Page Start:
3113
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗