Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome

• প্রধান লেখক: Chong Kun Cheon (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Korean Society of Pediatric Endocrinology, 2016-09-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

The Prader-Willi syndrome (PWS) is a human imprinting disorder resulting from genomic alterations that inactivate imprinted, paternally expressed genes in human chromosome region 15q11-q13. This genetic condition appears to be a contiguous gene syndrome caused by the loss of at least 2 of a number o...