Title: Prenatal detection of deletion–duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion
Abstract: Prenatal DiagnosisVolume 28, Issue 5 p. 466-468 Research Letter Prenatal detection of deletion–duplication of chromosome 3 arising from meiotic recombination of a familial pericentric inversion K. Prabhakara, Corresponding Author K. Prabhakara [email protected] Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, India Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaCytogenetics Laboratory, VCGS Pathology, 10th Floor, Royal Children's Hospital Parkville, Victoria 3052, Australia.Search for more papers by this authorDamien L. Bruno, Damien L. Bruno Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaSearch for more papers by this authorPriya Padman, Priya Padman Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaSearch for more papers by this authorSuma Prasad, Suma Prasad Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, IndiaSearch for more papers by this authorR. Sudheer Kumar, R. Sudheer Kumar Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, IndiaSearch for more papers by this authorHoward R. Slater, Howard R. Slater Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaSearch for more papers by this authorA. Radha Ramadevi, A. Radha Ramadevi Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, IndiaSearch for more papers by this author K. Prabhakara, Corresponding Author K. Prabhakara [email protected] Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, India Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaCytogenetics Laboratory, VCGS Pathology, 10th Floor, Royal Children's Hospital Parkville, Victoria 3052, Australia.Search for more papers by this authorDamien L. Bruno, Damien L. Bruno Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaSearch for more papers by this authorPriya Padman, Priya Padman Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaSearch for more papers by this authorSuma Prasad, Suma Prasad Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, IndiaSearch for more papers by this authorR. Sudheer Kumar, R. Sudheer Kumar Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, IndiaSearch for more papers by this authorHoward R. Slater, Howard R. Slater Cytogenetics Laboratory, VCGS Pathology, Royal Children's Hospital, Melbourne, Victoria, AustraliaSearch for more papers by this authorA. Radha Ramadevi, A. Radha Ramadevi Diagnostics Division, Center for DNA Fingerprinting and Diagnostics, Hyderabad, IndiaSearch for more papers by this author First published: 28 April 2008 https://doi.org/10.1002/pd.2005Citations: 3AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article.Citing Literature Volume28, Issue5May 2008Pages 466-468 RelatedInformation
Publication Year: 2008
Publication Date: 2008-04-28
Language: en
Type: letter
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 4
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