Ventricular septal defect genetics: Difference between revisions
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New page: {{SI}} {{CMG}} and Leida Perez, M.D. '''Associate Editor-in-Chief:''' Keri Shafer, M.D. [mailto:kshafer@bidmc.harvard.edu] {{EH}} ==Genetics== The frequent associa... |
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'''Associate Editor-in-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu] | '''Associate Editor-in-Chief:''' [[User:KeriShafer|Keri Shafer, M.D.]] [mailto:kshafer@bidmc.harvard.edu] | ||
==Genetics== | ==Genetics== |
Latest revision as of 17:20, 20 August 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] and Leida Perez, M.D.
Associate Editor-in-Chief: Keri Shafer, M.D. [2]
Genetics
The frequent association between arch abnormalities and significant conal VSDs suggests a common mechanism involving a chromosome band 22q11 microdeletion. Deletions in this area have not been linked with isolated supracristal VSDs.