The Etiology of Prader-Willi Syndrome: Clinical Implications of the Chromosome 15 Abnormalities
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4612-3854-6_2.pdf
Reference41 articles.
1. Berry, A. C., Wittingham, A. G., & Neville, B. G. R. (1981). Chromosome 15 in floppy infants. Archives of Disease in Childhood, 56, 882–885.
2. Bray, G. A., Dahms, W. T., Swerdloff, R. S., Fiser, R. H., Atkinson, R. L., & Carrel, R. E. (1983). The Prader-Willi syndrome: A study of 40 patients and a review of the literature. Medicine, 62, 59–80.
3. Butler, M. G., Meaney, F. J., & Palmer, C. G. (1986). Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. American Journal of Medical Genetics, 23, 793–809.
4. Cassidy, S. B, Thuline, H. C, & Holm, V. A. (1984). Deletion of chromosome 15(q11–13) in a Prader-Labhart-Willi syndrome clinic population. American Journal of Medical Genetics, 17, 485–495.
5. Cassidy, S. B. (1987). Letter to the Editor: Recurrence risk in Prader-Willi syndrome. American Journal of Medical Genetics, 28, 59–60.
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3. Personality profiles of youngsters with Prader-Willi syndrome and youngsters attending regular schools;Journal of Intellectual Disability Research;1995-06
4. Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics;American Journal of Medical Genetics;1995-02-13
5. Genetics of Prader—Willi Syndrome;Management of Prader-Willi Syndrome;1995
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