Chinese Siblings with Prader-Willi Syndrome Inherited from Their Paternal Grandmother
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s13312-019-1626-z.pdf
Reference10 articles.
1. Butler MG. Prader-Willi syndrome: Obesity due to genomic imprinting. Curr Genomics. 2011;12:204–15.
2. Rocha CF, Paiva CL. Prader-Willi-like phenotypes: A systematic review of their chromosomal abnormalities. Genet Mol Res. 2014;1:2290–8.
3. Cassidy SB, Driscoll DJ. Prader-Willi syndrome. Eur J Hum Genet. 2009;17:3–13.
4. Williams CA, Driscoll DJ, Dagli AI. Clinical and genetic aspects of Angelman syndrome. Genet Med. 2010;12: 385–95.
5. Buiting K, Gross S, Lich C, Gillessen-Kaesbach G, El-Maarri O, Horsthemke B. Epimutations in Prader-Willi and Angelman syndromes: A molecular study of 136 patients with an imprinting defect. Am J Hum Genet. 2003;72: 571–7.
Cited by 2 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
1. Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China;Orphanet Journal of Rare Diseases;2022-06-13
2. Prader-Willi Syndrome: Molecular Mechanism and Epigenetic Therapy;Current Gene Therapy;2020-06-24
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