Uniparental Disomy of Chromosome 15 in Two Cases by Chromosome Microarray: A Lesson Worth Thinking
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DOI: 10.1159/000477520
Abstract: Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are neurogenetic disorders caused by loss of function of the imprinted genes at 15q11q13. A 5-7 Mb paternal/maternal deletion of chromosomal region 15q11.2q13 is the major genetic cause… read more here.
Keywords: uniparental disomy; disomy chromosome; heteroupd isoupd; chromosome microarray ... See more keywords