- Title
- Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions
- Creators
- Raihan K Uddin - Department of Biology, University of Western Ontario, London, Ontario, N6A 5B7, CanadaYang Zhang - Department of Biology, University of Western Ontario, London, Ontario, N6A 5B7, CanadaVictoria Mok Siu - Division of Medical Genetics, University of Western Ontario, London, Ontario, N6A 5B7, CanadaYao-Shan Fan - Division of Medical Genetics, University of Western Ontario, London, Ontario, N6A 5B7, CanadaRichard L O'Reilly - Department of Psychiatry, University of Western Ontario, London, Ontario, N6A 5B7, CanadaJay Rao - Department of Psychiatry, University of Western Ontario, London, Ontario, N6A 5B7, CanadaShiva M Singh - Department of Biology, University of Western Ontario, London, Ontario, N6A 5B7, Canada
- Publication Details
- BMC medical genetics, Vol.7(1), pp.18-18
- Publisher
- BioMed Central
- Academic Unit
- Miller School of Medicine; UMMG Department of Pathology
- Language
- English
- Resource Type
- Journal article
- PMID
- 16512914
- PMCID
- PMC1413517
- Record Identifier
- 991031614861602976
Journal article
Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions
BMC medical genetics, Vol.7(1), pp.18-18
2006-03-02
PMCID: PMC1413517
PMID: 16512914
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- Citation topics
- 1 Clinical & Life Sciences
- 1.186 Chromosome Disorders
- 1.186.948 Digeorge Syndrome
- Web Of Science research areas
- Genetics & Heredity
- ESI research areas
- Molecular Biology & Genetics
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Source: InCites