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Talk:Arachnodactyly

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Wiki Education Foundation-supported course assignment

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This article is or was the subject of a Wiki Education Foundation-supported course assignment. Further details are available on the course page. Student editor(s): Mmillone.

Above undated message substituted from Template:Dashboard.wikiedu.org assignment by PrimeBOT (talk) 14:37, 16 January 2022 (UTC)Reply

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A possible source for the FBN1, FBN2 claim:

"A number of conditions related to Marfan syndrome are also due to FBN1 mutations. Contractural arachnodactyly is due to mutations in FBN2." From http://www.ncbi.nlm.nih.gov/pubmed/8541880  Preceding unsigned comment added by 76.230.240.234 (talk) 17:53, 27 January 2015 (UTC)Reply

Bibliography In Progress

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  • Medline Plus [1]
  • Trip Database Results [2]
  • Fibrillin Microfibrils in Bone Physiology [3]
  • Arachnodactyly--A Key to Diagnosing Heritable Disorders of Connective Tissue [4]
  • More PubMed Results [5]
  • Congenital Contractural Arachnodactyly (Beals Syndrome) [6]

Mmillone (talk) 22:03, 10 October 2015 (UTC)Reply

References

  1. "Arachnodactyly". Medline Plus. Retrieved 10 October 2015.
  2. "Trip Database". Trip Database. Retrieved 10 October 2015.
  3. Smaldone, S. "Fibrillin microfibrils in bone physiology". NCBI-PubMed. Retrieved 10 October 2015.
  4. Grahame, R. "Arachnodactyly--a key to diagnosing heritable disorders of connective tissue". NCBI-PubMed. Retrieved 10 October 2015.
  5. NCBI-PubMed http://www.ncbi.nlm.nih.gov/pubmed/?term=arachnodactyly. Retrieved 10 October 2015. {{cite web}}: Missing or empty |title= (help)
  6. NCBI-PMC http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524931/. Retrieved 10 October 2015. {{cite web}}: Missing or empty |title= (help)