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Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.
Saitta, Sulagna C; Harris, Stacy E; Gaeth, Ann P; Driscoll, Deborah A; McDonald-McGinn, Donna M; Maisenbacher, Melissa K; Yersak, Jill M; Chakraborty, Prabir K; Hacker, April M; Zackai, Elaine H; Ashley, Terry; Emanuel, Beverly S.
Affiliation
  • Saitta SC; Division of Human Genetics, The Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Hum Mol Genet ; 13(4): 417-28, 2004 Feb 15.
Article in En | MEDLINE | ID: mdl-14681306
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spermatocytes / Chromosomes, Human, Pair 22 / Gene Rearrangement / Chromosome Aberrations / DiGeorge Syndrome Limits: Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2004 Type: Article Affiliation country: United States
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spermatocytes / Chromosomes, Human, Pair 22 / Gene Rearrangement / Chromosome Aberrations / DiGeorge Syndrome Limits: Humans / Male Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2004 Type: Article Affiliation country: United States