High-resolution cytogenetic studies in patients with Prader-Willi syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb00603.x/fullpdf
Reference19 articles.
1. Parental origin of chromosome 15 deletion in Prader-Willi syndrome;Butler;Lancet,1983
2. Clinical and cytogenetical survey of 39 individuals with Prader-Labhart-Willi syndrome;Butler;Am. J. Med. Genet.,1986
3. Deletion of chromosome 15(qll-13) in a Prader-Labhart-Willi syndrome clinic population;Cassidy;Am. J. Med. Genet.,1984
4. Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment;Fraccaro;Hum. Genet.,1983
5. Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion;France;Clin. Genet.,1984
Cited by 15 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. Prader-Willi syndrome in two siblings: one with normal karyotype, one with a terminal deletion of distal Xq;Clinical Genetics;2008-06-28
2. The oro-dental phenotype in Prader?Willi syndrome: a survey of 15 patients;International Journal of Paediatric Dentistry;2007-07-23
3. A Multicenter Italian Study on Prader-Willi Syndrome;Prader-Willi Syndrome;1992
4. A catalogue of multiple congenital anomaly syndromes;Multiple Congenital Anomalies;1991
5. The Speech and Language Characteristics of Children with Prader-Willi Syndrome;Journal of Speech and Hearing Disorders;1990-05
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