The Prader-Willi syndrome and the Sotos syndrome: syndromes or sequences?
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb03481.x/fullpdf
Reference3 articles.
1. Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes;Beemer;Am. J. Med. Genet.,1986
2. Partial fra(X) phenotype with megalotestes in fra(X)-negative patients with acquired lesions of the central nervous system;Fryns;Am. J. Med. Genet.,1986
3. Prader-Willi syndrome in two siblings: one with normal karyotype, one with a terminal deletion of distal Xq;Ishikawa;Clin. Genet.,1987
Cited by 5 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. Differentiated recurrence risk estimations in the Prader-Willi syndrome;Clinical Genetics;2008-06-28
2. Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21));Clinical Genetics;2008-06-28
3. Prader-Willi syndrome and Sotos syndrome;Clinical Genetics;2008-06-28
4. Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13;American Journal of Medical Genetics;1992-11-01
5. The Speech and Language Characteristics of Children with Prader-Willi Syndrome;Journal of Speech and Hearing Disorders;1990-05
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