Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy.

Cartwright, Ashley

Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy. [electronic resource] - Clinical dysmorphology Jan 2017 - 38-40 p. digital

Publication Type: Case Reports; Journal Article

1473-5717

10.1097/MCD.0000000000000154 doi


Child
Chromosome Deletion
Chromosomes, Human, X
Comparative Genomic Hybridization
Developmental Disabilities--diagnosis
Facies
Genetic Association Studies
Humans
Male
Phenotype
p21-Activated Kinases--genetics