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q=%22q%3D%22 https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FFinger_%28disambiguation%29 from en.wikipedia.org
DiGeorge syndrome, also known as 22q11.2 deletion syndrome, is a syndrome caused by a microdeletion on the long arm of chromosome 22. While the symptoms can ...
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22q11.2 duplication syndrome is a rare genetic disorder caused by a duplication of a segment at the end of chromosome 22.
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Individuals with 22q11.2 deletion syndrome (22q11.2DS) can present with a wide range of features that are highly variable, even within families.
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q=%22q%3D%22 https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FFinger_%28disambiguation%29 from en.wikipedia.org
22q11.2 distal deletion syndrome is a rare genetic condition caused by a tiny missing part of one of the body's 46 chromosomes – chromosome 22.
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q=%22q%3D%22 https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FFinger_%28disambiguation%29 from www.mayoclinic.org
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 ...
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q=%22q%3D%22 https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FFinger_%28disambiguation%29 from medlineplus.gov
Dec 1, 2019 · 22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece ...
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The 22q11 region is involved in chromosomal rearrangements that lead to altered gene dosage, resulting in genomic disorders that are characterized by mental ...
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