Author:
Hogart Amber,Wu David,LaSalle Janine M.,Schanen N. Carolyn
Reference161 articles.
1. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes;Abeliovich;Eur. J. Hum. Genet.,1995
2. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization;Abuelo;Clin. Pediatr. (Phila),1995
3. Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons;Albrecht;Nat. Genet.,1997
4. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
5. Chromosome breakage in the Prader–Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints;Amos-Landgraf;Am. J. Hum. Genet.,1999
Cited by
224 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献