Comparative Frequency of Fragile-X (FMR1) and Creatine Transporter (SLC6A8) Mutations in X-Linked Mental Retardation

This publication has 11 references indexed in Scilit:

• Monogenic X-linked mental retardation: Is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations
  European Journal of Human Genetics, 2004
• Five years of molecular diagnosis of Fragile X syndrome (1997–2001): A collaborative study reporting 95% of the activity in France
  American Journal of Medical Genetics Part A, 2004
• High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation
  American Journal of Human Genetics, 2004
• Screening of the ARX gene in 682 retarded males
  European Journal of Human Genetics, 2004
• Molecular Screening of FRAXA and FRAXE in Indian Patients with Unexplained Mental Retardation
  Genetic Testing, 2002
• Screening for fragile X syndrome: results from a school for mentally retarded children
  Acta Paediatrica, 2002
• Screening for fragile X syndrome: results from a school for mentally retarded children
  Acta Paediatrica, 2002
• X-Linked Creatine-Transporter Gene (SLC6A8) Defect: A New Creatine-Deficiency Syndrome
  American Journal of Human Genetics, 2001
• Screening and Diagnosis for the Fragile X Syndrome among the Mentally Retarded: An Epidemiological and Psychological Survey
  American Journal of Human Genetics, 1997
• The diagnosis and frequency of X‐linked conditions in a cohort of moderately retarded males with affected brothers
  American Journal of Medical Genetics, 1983