Author:
Dalm Virgil A. S. H.,Driessen Gertjan J. A.,Barendregt Barbara H.,van Hagen Petrus M.,van der Burg Mirjam
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Reference41 articles.
1. Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study. Hum Hered. 1973;23(6):568–85.
2. Grossfeld PD, Mattina T, Lai Z, Favier R, Jones KL, Cotter F, et al. The 11q terminal deletion disorder: a prospective study of 110 cases. Am J Med Genet A. 2004;129A(1):51–61.
3. Penny LA, Dell’Aquila M, Jones MC, Bergoffen J, Cunniff C, Fryns JP, et al. Clinical and molecular characterization of patients with distal 11q deletions. Am J Hum Genet. 1995;56(3):676–83.
4. Pivnick EK, Velagaleti GV, Wilroy RS, Smith ME, Rose SR, Tipton RE, et al. Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases. J Med Genet. 1996;33(9):772–8.
5. Bernaciak J, Szczaluba K, Derwinska K, Wisniowiecka-Kowalnik B, Bocian E, Sasiadek MM, et al. Clinical and molecular-cytogenetic evaluation of a family with partial Jacobsen syndrome without thrombocytopenia caused by an approximately 5 Mb deletion del(11)(q24.3). Am J Med Genet A. 2008;146A(19):2449–54.
Cited by
27 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