Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delay

Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion

(2011) Georg M. Stettner et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

(2010) Angela L Duker et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The genetic basis of non-syndromic intellectual disability: a review

(2010) Liana Kaufman et al.   Journal of Neurodevelopmental Disorders

Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2

(2009) BC Ballif et al.   CLINICAL GENETICS

FRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structure

(2009) Mounia Bensaid et al.   NUCLEIC ACIDS RESEARCH

Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report

(2009) Ryan N Traylor et al.   Molecular Cytogenetics