Publications

Export 2 results:
Author Title [ Year(Asc)]
Filters: Author is Cecchi, Alana C and Keyword is Child  [Clear All Filters]
2020
Pinard, A. et al. The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. Genet Med 22, 427-431 (2020).
2014
Cecchi, A. C. et al. RNF213 rare variants in an ethnically diverse population with Moyamoya disease. Stroke 45, 3200-7 (2014).