Fragile X Syndrome in Korea: A Case Series and a Review of the Literature
Open Access
- 1 January 2008
- journal article
- case report
- Published by XMLink in Journal of Korean Medical Science
- Vol. 23 (3), 470-476
- https://doi.org/10.3346/jkms.2008.23.3.470
Abstract
Yim SY, et al. J Korean Med Sci. 2008 Jun;23(3):470-476. http://dx.doi.org/10.3346/jkms.2008.23.3.470Keywords
This publication has 24 references indexed in Scilit:
- Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndromeBrain Research Reviews, 2007
- Mosaicism for a full mutation, premutation, and deletion of the CGG repeats results in 22% FMRP and elevated FMR1 mRNA levels in a high‐functioning fragile X maleAmerican Journal of Medical Genetics Part A, 2006
- Fragile X SyndromePediatrics in Review, 2005
- A neuropsychological investigation of male premutation carriers of fragile X syndromeNeuropsychologia, 2004
- Clinical features of boys with fragile X premutations and intermediate allelesNeuropsychiatric Genetics, Part B of the American Journal of Medical Genetics (AJMG), 2003
- Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate AllelesAmerican Journal of Human Genetics, 2003
- Prevalence of the fragile X syndrome in African‐AmericansAmerican Journal of Medical Genetics, 2002
- Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: A laboratory protocolMolecular Diagnosis, 2000
- Molecular evidence that fragile X syndrome occurs in the South African black population.Journal of Medical Genetics, 1998
- Fragile‐X syndrome in North East Essex: towards systematic screening: clinical selectionJournal of Intellectual Disability Research, 1994