Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Erdel M., Schuffenhauer S., Buchholz B., Barth-Witte U., Köchl S., Utermann B., Duba H. C., Utermann G. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10). Hum Genet. 1996 Jun;97(6):784–793. doi: 10.1007/BF02346190. [DOI] [PubMed] [Google Scholar]
- Gillessen-Kaesbach G., Gross S., Kaya-Westerloh S., Passarge E., Horsthemke B. DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome. J Med Genet. 1995 Feb;32(2):88–92. doi: 10.1136/jmg.32.2.88. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holm V. A., Cassidy S. B., Butler M. G., Hanchett J. M., Greenswag L. R., Whitman B. Y., Greenberg F. Prader-Willi syndrome: consensus diagnostic criteria. Pediatrics. 1993 Feb;91(2):398–402. [PMC free article] [PubMed] [Google Scholar]
- Robinson W. P., Bottani A., Xie Y. G., Balakrishman J., Binkert F., Mächler M., Prader A., Schinzel A. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients. Am J Hum Genet. 1991 Dec;49(6):1219–1234. [PMC free article] [PubMed] [Google Scholar]
- Smith A., Prasad M., Deng Z. M., Robson L., Woodage T., Trent R. J. Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes. Arch Dis Child. 1995 May;72(5):397–402. doi: 10.1136/adc.72.5.397. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Williams C. A., Angelman H., Clayton-Smith J., Driscoll D. J., Hendrickson J. E., Knoll J. H., Magenis R. E., Schinzel A., Wagstaff J., Whidden E. M. Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation. Am J Med Genet. 1995 Mar 27;56(2):237–238. doi: 10.1002/ajmg.1320560224. [DOI] [PubMed] [Google Scholar]