Comprehensive analysis of Wolf–Hirschhorn syndrome using array CGH indicates a high prevalence of translocations
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://www.nature.com/articles/5201915.pdf
Reference30 articles.
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2. Lurie IW, Lazjuk GI, Ussova YI, Presman EB, Gurevich DB : The Wolf–Hirschhorn syndrome. Clin Genet 1980; 17: 375–384.
3. Zollino M, Di Stefano C, Zampino G et al: Genotype–phenotype correlations and clinical diagnostic criteria in Wolf–Hirschhorn syndrome. Am J Med Genet 2000; 94: 254–261.
4. Wieczorek D, Krause M, Majewski F et al: Effect of the size of the deletion and clinical manifestation in Wolf–Hirschhorn syndrome: analysis of 13 patients with a de novo deletion. Eur J Hum Genet 2000; 8: 519–526.
5. Estabrooks LL, Rao KW, Driscoll DA et al: Preliminary phenotypic map of chromosome 4p16 based on 4p deletions. Am J Med Genet 1995; 57: 581–586.
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