What is 22q11.2 Deletion Syndrome? Jennifer M. Granholm, Governor Janet Olszewski, Director 22q11.2 deletion syndrome is a genetic condition that affects learning, health, and physical traits. It occurs in males and fema

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Date: 2012-12-07 20:46:27 DiGeorge syndrome Chromosome 22 Cleft lip and palate Trisomy 22 22q11.2 duplication syndrome Health Syndromes Genetics		What is 22q11.2 Deletion Syndrome? Jennifer M. Granholm, Governor Janet Olszewski, Director 22q11.2 deletion syndrome is a genetic condition that affects learning, health, and physical traits. It occurs in males and fema Add to Reading List Source URL: www.michigan.gov Download Document from Source Website File Size: 167,17 KB Share Document on Facebook

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	ABOUT C22C Chromosome 22 was the first chromosome to be sequenced in the Human Genome Project. Beyond the conditions listed in this brochure, chromosome 22 has also been researched as a link to bi-polar disorder, schizop DocID: 1ahHZ - View Document
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	Velo-Cardio-Facial Syndrome Alternative names 22q11.2 deletion syndrome, Sedlackova syndrome, DiGeorge syndrome, Shprintzen syndrome, Conotruncal anomaly face syndrome. Genetics / aetiology 85-90% of individuals with VCF DocID: 19i6T - View Document