to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays.
Clinical utility of the X-chromosome array.
Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome.
A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features.
CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity.
SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability.
Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families.