Chromosome 1, deletion q21 q25: Difference between revisions

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==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


Revision as of 21:20, 22 July 2012

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2], Raviteja Guddeti, M.B.B.S.[3]

Overview

A rare chromosomal disorder where deletion of a portion of chromosome 1 results in various abnormalities such as retarded fetal growth, facial anomalies, osteoporosis, mental retardation and hearing loss.[1]


References

  1. ↑ Beemer FA, Klep-de Pater JM, Sepers GJ, Janssen B (1985). "Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43)". Clin. Genet. 27 (5): 515–9. PMID 4006278. Unknown parameter |month= ignored (help)



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