Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances-Reference-Cited by-同舟云学术

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances

Published:2009-03 Issue:2-3 Volume:52 Page:108-115
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Doornbos Marianne,Sikkema-Raddatz Birgit,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. (Mieke),van Essen Ton,Kok Klaas,van Silfhout Anneke T.,Breuning Martijn,van Ravenswaaij-Arts Conny M.A.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference17 articles.

1. Subtelomeric imbalances in phenotypically normal individuals;Balikova;Hum. Mutat.,2007

2. Prader–Willi syndrome: clinical genetics, cytogenetics and molecular biology;Bittel;Expert Rev. Mol. Med.,2005

3. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader–Willi syndrome;Bittel;Pediatrics,2006

4. Behavioural differences among subjects with Prader–Willi syndrome and type I or type II deletion and maternal disomy;Butler;Pediatrics,2004

5. Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader–Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons;Chai;Am. J. Hum. Genet.,2003

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