Including results for gbv=1 %22q11%3D%22 sa%253DX
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Abstract. 22q11.2 deletion syndrome is one of the most common microdeletion syndromes. Most patients have a deletion resulting from a recombination of low copy ...
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The diagnosis of 22q11.2DS is established in a proband by identification of a heterozygous deletion at chromosome 22q11.2 (see Table 1). The majority of ...
Missing: gbv= 3D% 253DX
DiGeorge syndrome (22q11.2 deletion syndrome) - Symptoms and causes
www.mayoclinic.org › syc-20353543
Jan 13, 2024 · This condition is due to missing part of chromosome 22. It may cause heart issues, thyroid problems, cleft palate, lower immunity and other ...
Missing: gbv= 3D% sa% 253DX
2 distal deletion is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22. For healthy development, ...
Missing: 3D% sa% 253DX
A genetic disorder caused by the partial deletion of genetic material on one copy of a person's chromosome 22.
Missing: 3D% sa% 253DX
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