Phenotypic features in patients with 15q11.2(BP1-BP2) deletion: Further delineation of an emerging syndrome
Author:
Affiliation:
1. Department of Medical and Molecular Genetics; King's College; London UK
2. Guy's & St Thomas' NHS Foundation Trust; London UK
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36554/fullpdf
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3. Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance;Ahn;Mol Cytogenet,2010
4. Mapping autism risk loci using genetic linkage and chromosomal rearrangements;Szatmari;Nat Genet,2007
5. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome;Bittel;Pediatrics,2006
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