Talk:Arachnodactyly
Latest comment: 2 years ago by PrimeBOT in topic Wiki Education Foundation-supported course assignment
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Wiki Education Foundation-supported course assignment
editThis 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
editA 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
edit- 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)
References
- ^ "Arachnodactyly". Medline Plus. Retrieved 10 October 2015.
- ^ "Trip Database". Trip Database. Retrieved 10 October 2015.
- ^ Smaldone, S. "Fibrillin microfibrils in bone physiology". NCBI-PubMed. Retrieved 10 October 2015.
- ^ Grahame, R. "Arachnodactyly--a key to diagnosing heritable disorders of connective tissue". NCBI-PubMed. Retrieved 10 October 2015.
- ^ NCBI-PubMed http://www.ncbi.nlm.nih.gov/pubmed/?term=arachnodactyly. Retrieved 10 October 2015.
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(help) - ^ NCBI-PMC http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524931/. Retrieved 10 October 2015.
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