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Autor:
Daniel E. Pineda-Alvarez, Ludmila Matyakhina, G. Shashidhar Pai, Mohammed Al Balwi, Stephen R. Braddock, Jeanne Meck, Dongli Huang, Jessica Niet, Leigh D. deHoll, Dianalee McKnight, Brenda Cristina Rios Valdez, Courtney Downtain
Publikováno v:
Cancer Genetics. 209:238
Prader-Willi (PWS) and Angelman (AS) syndromes are genetic disorders with multiple well-known mechanisms. Approximately 70% of individuals with PWS or AS have a ~4 Mb deletion of 15q11-q13, while the remainder have UPD15, an imprinting defect or, in