Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature

M Assoum, AL Bruel, ML Crenshaw… - American Journal of …, 2020 - Wiley Online Library
Abstract In 2011, KIAA1033/WASHC4 was associated with autosomal recessive intellectual
disability (ARID) in a large consanguineous family comprising seven affected individuals …
被引用次数：12 相关文章

Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature

M Assoum, AL Bruel, ML Crenshaw… - American Journal of …, 2020 - pure.johnshopkins.edu
Abstract In 2011, KIAA1033/WASHC4 was associated with autosomal recessive intellectual
disability (ARID) in a large consanguineous family comprising seven affected individuals …

Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature.

M Assoum, AL Bruel, ML Crenshaw… - American Journal of …, 2020 - europepmc.org
In 2011, KIAA1033/WASHC4 was associated with autosomal recessive intellectual disability
(ARID) in a large consanguineous family comprising seven affected individuals with …

Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature

M Assoum, AL Bruel, ML Crenshaw… - … journal of medical …, 2020 - pubmed.ncbi.nlm.nih.gov
In 2011, KIAA1033/WASHC4 was associated with autosomal recessive intellectual disability
(ARID) in a large consanguineous family comprising seven affected individuals with …

Novel KIAA1033/WASHC4 mutations in three patients with syndromic intellectual disability and a review of the literature

M Assoum, AL Bruel, ML Crenshaw, J Delanne… - American Journal of …, 2020 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> In 2011,< jats: italic> KIAA1033</jats: italic>/<
jats: italic> WASHC4</jats: italic> was associated with autosomal recessive intellectual …