Author:
Vogels Annick,Van Den Ende Jenneke,Keymolen Kathelijne,Mortier Geert,Devriendt Koen,Legius E,Fryns J P
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference16 articles.
1. Cassidy SB : Prader–Willi syndrome. J Med Genet 1997; 34: 917–923.
2. Ledbetter DH, Riccardi VM, Airhart SD, Strobel RJ, Keenan BS, Crawford JD : Deletions of chromosome 15 as a cause of the Prader–Willi syndrome. N Engl J Med 1981; 304: 325–329.
3. Nicholls RD, Knoll JH, Butler MG, Karam S, Lalande M : Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader–Willi syndrome. Nature 1989; 342: 281–285.
4. Robinson WP, Bottani A, Xie YG et al: Molecular, cytogenetic, and clinical investigations of Prader–Willi syndrome patients. Am J Hum Genet 1991; 49: 1219–1234.
5. Buiting K, Saitoh S, Gross S et al: Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet 1995; 9: 395–400.
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