Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder
Year: 1998
Type: article
Study design: Observational Study
Source: The Journal of Pediatrics
Authors: Gretchen A. Meyer, Nathan J. Blum, Wendy Hitchcock, Paolo Fortina
Institution: Naval Medical Center Portsmouth
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W2072157333
