Chromosome 1, deletion q21 q25: Difference between revisions
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Created page with "__NOTOC__ {{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, Raviteja Guddeti, M.B.B.S.[mailto:rgudetti@perfuse.org] ==Overview== A rare ch..." |
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__NOTOC__ | __NOTOC__ | ||
{{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, [[User:Raviteja Reddy Guddeti|Raviteja Guddeti, M.B.B.S.]][mailto: | {{CMG}}; '''Associate Editor(s)-In-Chief:''' {{CZ}}, [[User:Raviteja Reddy Guddeti|Raviteja Guddeti, M.B.B.S.]][mailto:ravitheja.g@gmail.com] | ||
==Overview== | ==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.<ref name="pmid4006278">{{cite journal |author=Beemer FA, Klep-de Pater JM, Sepers GJ, Janssen B |title=Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43) |journal=Clin. Genet. |volume=27 |issue=5 |pages=515–9 |year=1985 |month=May |pmid=4006278 |doi= |url=}}</ref> | 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.<ref name="pmid4006278">{{cite journal |author=Beemer FA, Klep-de Pater JM, Sepers GJ, Janssen B |title=Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43) |journal=Clin. Genet. |volume=27 |issue=5 |pages=515–9 |year=1985 |month=May |pmid=4006278 |doi= |url=}}</ref> | ||
==References== | |||
{{Reflist|2}} | {{Reflist|2}} | ||
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[[Category:Genetics]] | [[Category:Genetics]] | ||
{{WikiDoc Help Menu}} | {{WikiDoc Help Menu}} | ||
{{WikiDoc Sources}} | {{WikiDoc Sources}} | ||
Latest revision as of 01:20, 2 November 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