Latest Autism Paper:De novo interstitial duplication of 15q11.2–q13.1 with complex maternal uniparental trisomy for the 15q11–q13 region in a patient with Prader–Willi syndrome
Summary Prader–Willi syndrome is brought on by the absence of paternal contribution for the imprinted 15q11–q13 area that originates by means of a variety of mechanisms these kinds of as paternal deletion of 15q11–q13, maternal uniparental disomy, or by an imprinting defect because of to epimutations in the paternal imprinting middle. In the existing report, [...]