Fragile X syndrome (Simple English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fragile X syndrome" in Simple English language version.

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annualreviews.org

Santoro M.R. et al 2012. Molecular mechanisms of Fragile X Syndrome: a twenty-year perspective. Annu. Rev. Pathol. Mech. Dis. 7: 219–45. [1] Archived 2016-05-23 at the Wayback Machine

cdc.gov

CDC (2022-06-03). "What is Fragile X Syndrome (FXS)? | CDC". Centers for Disease Control and Prevention. Retrieved 2023-01-11.

doi.org

McLennan Y. et al 2011 (2011). "Fragile X Syndrome". Current Genomics. 12 (3): 216–224. doi:10.2174/138920211795677886. PMC 3137006. PMID 22043169.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Budimirovic D.B. & Kaufmann W.E. 2011 (2011). "What can we learn about autism from studying fragile X syndrome?". Dev Neurosci. 33 (5): 379–94. doi:10.1159/000330213. PMC 3254037. PMID 21893949. Retrieved 26 January 2012.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Maddalena A. et al 2001. (2001). "Technical Standards and Guidelines for Fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics". Genetics in Medicine. 3 (3): 200–205. doi:10.1097/00125817-200105000-00010. PMC 3110344. PMID 11388762.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Nolin S.L. et al 2003 (2003). "Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles". American Journal of Human Genetics. 72 (2): 454–64. doi:10.1086/367713. PMC 379237. PMID 12529854.{{cite journal}}: CS1 maint: numeric names: authors list (link)

karger.com

content.karger.com

Budimirovic D.B. & Kaufmann W.E. 2011 (2011). "What can we learn about autism from studying fragile X syndrome?". Dev Neurosci. 33 (5): 379–94. doi:10.1159/000330213. PMC 3254037. PMID 21893949. Retrieved 26 January 2012.{{cite journal}}: CS1 maint: numeric names: authors list (link)

nih.gov

ncbi.nlm.nih.gov

McLennan Y. et al 2011 (2011). "Fragile X Syndrome". Current Genomics. 12 (3): 216–224. doi:10.2174/138920211795677886. PMC 3137006. PMID 22043169.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Budimirovic D.B. & Kaufmann W.E. 2011 (2011). "What can we learn about autism from studying fragile X syndrome?". Dev Neurosci. 33 (5): 379–94. doi:10.1159/000330213. PMC 3254037. PMID 21893949. Retrieved 26 January 2012.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Maddalena A. et al 2001. (2001). "Technical Standards and Guidelines for Fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics". Genetics in Medicine. 3 (3): 200–205. doi:10.1097/00125817-200105000-00010. PMC 3110344. PMID 11388762.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Nolin S.L. et al 2003 (2003). "Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles". American Journal of Human Genetics. 72 (2): 454–64. doi:10.1086/367713. PMC 379237. PMID 12529854.{{cite journal}}: CS1 maint: numeric names: authors list (link)

pubmed.ncbi.nlm.nih.gov

McLennan Y. et al 2011 (2011). "Fragile X Syndrome". Current Genomics. 12 (3): 216–224. doi:10.2174/138920211795677886. PMC 3137006. PMID 22043169.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Budimirovic D.B. & Kaufmann W.E. 2011 (2011). "What can we learn about autism from studying fragile X syndrome?". Dev Neurosci. 33 (5): 379–94. doi:10.1159/000330213. PMC 3254037. PMID 21893949. Retrieved 26 January 2012.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Maddalena A. et al 2001. (2001). "Technical Standards and Guidelines for Fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics". Genetics in Medicine. 3 (3): 200–205. doi:10.1097/00125817-200105000-00010. PMC 3110344. PMID 11388762.{{cite journal}}: CS1 maint: numeric names: authors list (link)
Nolin S.L. et al 2003 (2003). "Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles". American Journal of Human Genetics. 72 (2): 454–64. doi:10.1086/367713. PMC 379237. PMID 12529854.{{cite journal}}: CS1 maint: numeric names: authors list (link)

web.archive.org

Santoro M.R. et al 2012. Molecular mechanisms of Fragile X Syndrome: a twenty-year perspective. Annu. Rev. Pathol. Mech. Dis. 7: 219–45. [1] Archived 2016-05-23 at the Wayback Machine