Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability
- 1 June 2010
- journal article
- research article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 86 (6) , 892-903
Abstract
No abstract availableKeywords
Funding Information
- Belgian Federal Science Policy Office
- Intellectual and Developmental Disabilities Research Center (P30HD024064)
- Fonds Wetenschappelijk Onderzoek (P6/43)
- Deutsches Krebsforschungszentrum (M01RR00188)
- Ministerstvo Zdravotnictví Ceské Republiky (IGA NS 10554-3)
- Ministry of Education of the People's Republic of China (NCET-09-0322)
- Universiteit Antwerpen
- Bundesministerium für Forschung, Technologie und Raumfahrt (01ES0815)
- Fonds De La Recherche Scientifique - FNRS
- National Institute of Neurological Disorders and Stroke
- National Institutes of Health (R01NS058529)
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