Results 191 to 200 of about 27,851 (250)

Whole-Exome Sequencing Identifies Novel Genetic Variants Associated with Unexplained Neurodevelopmental Disorders in Children. [PDF]

open access: yesInt J Mol Sci
Mancuso G   +13 more
europepmc   +1 more source

Potential Link Between a Disruptive <i>CAPN6</i> Variant and Neurodevelopmental Disorders. [PDF]

open access: yesInt J Mol Sci
Calì F   +15 more
europepmc   +1 more source

Impact of low vision and blindness on characteristics of developmental delay in children younger than 6 years. [PDF]

open access: yesWorld J Clin Pediatr
Wannapaschaiyong P   +14 more
europepmc   +1 more source

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