Hi, I am Levi, I am 18 years old, and I have 22Q11 deletion syndrome. I was born with a congenital heart condition called Truncus Arteriosis Type II, ...
Missing: q 3D% https% 3A% 2Foag. 2Ffingerprints% 2Frecord- review% 2Fcert- copies
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The major clinical manifestations of 22q11.2DS include congenital heart disease, particularly conotruncal malformations (ventricular septal defect, tetralogy of ...
Missing: 3D% 3A% 2Foag. 2Ffingerprints% 2Frecord- 2Fcert-
22q11.2 deletion syndrome is a genetic condition that causes a combination of medical problems. These problems can vary widely from child to child, ...
Most cases result from a deletion of chromosome 22q11.2 (the DiGeorge syndrome chromosome region, or DGCR). Several genes are lost including the putative ...
In the present review, we focus on efforts to determine both the mechanism for the rearrangements and the molecular basis of these disorders. Clinical and ...
22q11DS is a deletion of 1.5 to 3 Mb on the long (q) arm of chromosome 22. ... 2++ High quality systematic reviews of case ... Chromosome 22-specific low copy ...
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