Publications

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Author Title [ Year(Desc)]
Filters: Author is Aldinger, Kimberly A and Keyword is Child, Preschool  [Clear All Filters]
2014
Aldinger, K. A. et al. Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy. Am J Hum Genet 95, 227-34 (2014).
2020
Mirzaa, G. M. et al. De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder. Genet Med 22, 538-546 (2020).