Talk:Arachnodactyly

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)

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)

Bibliography In Progress
Mmillone (talk) 22:03, 10 October 2015 (UTC)
 * Medline Plus
 * Trip Database Results
 * Fibrillin Microfibrils in Bone Physiology
 * Arachnodactyly--A Key to Diagnosing Heritable Disorders of Connective Tissue
 * More PubMed Results
 * Congenital Contractural Arachnodactyly (Beals Syndrome)