Talk:Arachnodactyly

From WikiProjectMed
Jump to navigation Jump to search

Wiki Education Foundation-supported course assignment

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]

Untitled

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

  • 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)
Retrieved from "https://mdwiki.org/wiki/Talk:Arachnodactyly"