Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy
2009; Wiley; Volume: 149A; Issue: 4 Linguagem: Inglês
10.1002/ajmg.a.32463
ISSN1552-4833
AutoresMeena Balasubramanian, John Barber, Morag N. Collinson, Shuwen Huang, Viv Maloney, Dave Bunyan, Nicki Foulds,
Tópico(s)Chronic Lymphocytic Leukemia Research
ResumoAmerican Journal of Medical Genetics Part AVolume 149A, Issue 4 p. 793-797 Research Letter Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy† Meena Balasubramanian, Corresponding Author Meena Balasubramanian [email protected] Wessex Clinical Genetics Service, Southampton University Hospitals Trust, Princess Anne Hospital, Southampton, UKWessex Clinical Genetics Service, Southampton University Hospitals Trust, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK.Search for more papers by this authorJohn C.K. Barber, John C.K. Barber Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK National Genetics Reference Laboratory (Wessex), Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK Human Genetics Division, Southampton University Hospitals Trust, Southampton, UKSearch for more papers by this authorMorag N. Collinson, Morag N. Collinson Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorShuwen Huang, Shuwen Huang National Genetics Reference Laboratory (Wessex), Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorViv K. Maloney, Viv K. Maloney National Genetics Reference Laboratory (Wessex), Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorDave Bunyan, Dave Bunyan Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorNicki Foulds, Nicki Foulds Wessex Clinical Genetics Service, Southampton University Hospitals Trust, Princess Anne Hospital, Southampton, UKSearch for more papers by this author Meena Balasubramanian, Corresponding Author Meena Balasubramanian [email protected] Wessex Clinical Genetics Service, Southampton University Hospitals Trust, Princess Anne Hospital, Southampton, UKWessex Clinical Genetics Service, Southampton University Hospitals Trust, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, UK.Search for more papers by this authorJohn C.K. Barber, John C.K. Barber Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK National Genetics Reference Laboratory (Wessex), Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UK Human Genetics Division, Southampton University Hospitals Trust, Southampton, UKSearch for more papers by this authorMorag N. Collinson, Morag N. Collinson Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorShuwen Huang, Shuwen Huang National Genetics Reference Laboratory (Wessex), Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorViv K. Maloney, Viv K. Maloney National Genetics Reference Laboratory (Wessex), Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorDave Bunyan, Dave Bunyan Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury District Hospital, Salisbury, UKSearch for more papers by this authorNicki Foulds, Nicki Foulds Wessex Clinical Genetics Service, Southampton University Hospitals Trust, Princess Anne Hospital, Southampton, UKSearch for more papers by this author First published: 24 March 2009 https://doi.org/10.1002/ajmg.a.32463Citations: 14 † How to cite this article: Balasubramanian M, Barber JCK, Collinson MN, Huang S, Maloney VK, Bunyan D, Foulds N. 2009. Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy. Am J Med Genet Part A 149A:793–797. Read the full textAboutPDF 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 Citing Literature Volume149A, Issue4April 2009Pages 793-797 RelatedInformation
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