Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay-Reference-Cited by-同舟云学术

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

Published:2011-02-27 Issue:4 Volume:130 Page:517-528
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Burnside Rachel D.,Pasion Romela,Mikhail Fady M.,Carroll Andrew J.,Robin Nathaniel H.,Youngs Erin L.,Gadi Inder K.,Keitges Elizabeth,Jaswaney Vikram L.,Papenhausen Peter R.,Potluri Venkateswara R.,Risheg Hiba,Rush Brooke,Smith Janice L.,Schwartz Stuart,Tepperberg James H.,Butler Merlin G.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-011-0970-4.pdf

Reference47 articles.

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2. Baldwin EL, Lee JY, Blake DM, Bunke BP, Alexander CR, Kogan AL, Ledbetter DH, Martin CL (2008) Enhanced detection of clinically relevant genomic imbalances using a targeted plus whole genome oligonucleotide microarray. Genet Med 10:415–429

3. Bittel DC, Kibiryeva N, Butler MG (2006) Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome. Pediatrics 118:e1276–e1283

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5. Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T (2004) Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy. Pediatrics 113:565–573

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