Author:
Chantot-Bastaraud Sandra,Stratmann Svea,Brioude Frédéric,Begemann Matthias,Elbracht Miriam,Graul-Neumann Luitgard,Harbison Madeleine,Netchine Irène,Eggermann Thomas
Funder
Bundesministerium für Bildung und Forschung
European Cooperation in Science and Technology
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Reference26 articles.
1. Hassold T, Hall H, Hunt P. The origin of human aneuploidy: where we have been, where we are going. Hum Mol Genet. 2007; Spec No. 2:R203–8.
2. Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, et al. An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. PLoS One. 2014;9:e99560.
3. Kotzot D, Utermann G. Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated. Am J Med Genet A. 2005;136:287–305.
4. Eggermann T, Netchine I, Temple K, Tümer Z, Monk D, Mackay D, Grønskov K, Riccio A, Linglart A, Maher ER. Congenital imprinting disorders: EUCID.Net – a network to decipher their aetiology and Congenital imprinting disorderic and clinical care. Clin. Epigenetics. 2015;7:123.
5. Eggermann T, Soellner L, Buiting K, Kotzot D. Uniparental Disomy and mosaicism in context with pregnancy. Trends Mol Med. 2015;21(2):77–87.
Cited by
10 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