Apr 24, 2024 · 2 Foundation is a nonprofit organization dedicated to supporting the needs of families and individuals affected by chromosome 22q11.2 ...
Missing: 3D% 3A% 2Foeksound.
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2DS) can present with a wide range of features that are highly variable, even within families. The major clinical manifestations of 22q11.2DS include congenital ...
Missing: 3D% 3A% 2Foeksound.
May 6, 2019 · 2 deletion syndrome (22q11.2DS) is caused by recurrent, chromosome specific, low copy repeat mediated copy number losses of chromosome 22q11.
Missing: 2Foeksound. | Show results with:2Foeksound.
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