Chromosome 1, deletion q21 q25: Difference between revisions
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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== | ||
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