Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader―Willi critical region, possibly associated with behavioural disturbances: Emerging Microdeletion and Microduplication Syndromes

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Bibliographic Details
Published in:European journal of medical genetics 2009, Vol.52 (2-3), p.108-115
Main Authors: DOORNBOS, Marianne, SIKKEMA-RADDATZ, Birgit, VAN ESSEN, Ton, KOK, Klaas, VAN SILFHOUT, Anneke T, BREUNING, Martijn, VAN RAVENSWAAIJ-ARTS, Conny M. A, RUIJVENKAMP, Claudia A. L, DIJKHUIZEN, Trijnie, BIJLSMA, Emilia K, GIJSBERS, Antoinet C. J, HILHORST-HOFSTEE, Yvonne, HORDIJK, Roel, VERBRUGGEN, Krijn T, KERSTJENS-FREDERIKSE, W. S
Format: Article
Language:English
Subjects:
Biological and medical sciences
Chromosome aberrations
Fundamental and applied biological sciences. Psychology
General aspects. Genetic counseling
Genetics of eukaryotes. Biological and molecular evolution
Medical genetics
Medical sciences
Metabolic diseases
Obesity
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ISSN:1769-7212
1878-0849