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Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long-Standing Clinical Utility of FISH.

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Title: Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long-Standing Clinical Utility of FISH.
Authors: Bryant LM; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA., Hokanson R; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA., Hickey SE; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA., Zapanta B; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA., Hunter J; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.; The Ohio State University Columbus Ohio USA., Reshmi SC; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.; The Ohio State University Columbus Ohio USA.
Source: Clinical case reports [Clin Case Rep] 2025 Nov 14; Vol. 13 (11), pp. e71483. Date of Electronic Publication: 2025 Nov 14 (Print Publication: 2025).
Publication Type: Journal Article
Journal Info: Publisher: John Wiley & Sons Country of Publication: England NLM ID: 101620385 Publication Model: eCollection Cited Medium: Print ISSN: 2050-0904 (Print) Linking ISSN: 20500904 NLM ISO Abbreviation: Clin Case Rep Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Familial 22q11.2 Duplication/Deletion Syndrome: A Testament to the Long-Standing Clinical Utility of FISH.
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  Data: <searchLink fieldCode="AU" term="%22Bryant+LM%22">Bryant LM</searchLink>; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.<br /><searchLink fieldCode="AU" term="%22Hokanson+R%22">Hokanson R</searchLink>; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.<br /><searchLink fieldCode="AU" term="%22Hickey+SE%22">Hickey SE</searchLink>; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.<br /><searchLink fieldCode="AU" term="%22Zapanta+B%22">Zapanta B</searchLink>; Department of Pediatrics, Section of Genetic and Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.<br /><searchLink fieldCode="AU" term="%22Hunter+J%22">Hunter J</searchLink>; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.; The Ohio State University Columbus Ohio USA.<br /><searchLink fieldCode="AU" term="%22Reshmi+SC%22">Reshmi SC</searchLink>; The Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital Columbus Ohio USA.; Department of Pediatrics The Ohio State University Columbus Ohio USA.; The Ohio State University Columbus Ohio USA.
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  Data: <searchLink fieldCode="JN" term="%22101620385%22">Clinical case reports</searchLink> [Clin Case Rep] 2025 Nov 14; Vol. 13 (11), pp. e71483. <i>Date of Electronic Publication: </i>2025 Nov 14 (<i>Print Publication: </i>2025).
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