Author:
Feenstra Ilse,Hanemaaijer Nicolien,Sikkema-Raddatz Birgit,Yntema Helger,Dijkhuizen Trijnie,Lugtenberg Dorien,Verheij Joke,Green Andrew,Hordijk Roel,Reardon William,Vries Bert de,Brunner Han,Bongers Ernie,Leeuw Nicole de,van Ravenswaaij-Arts Conny
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference34 articles.
1. Jacobs PA, Browne C, Gregson N, Joyce C, White H : Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. J Med Genet 1992; 29: 103–108.
2. Gardner RJMS, Sutherland GR : Chromosome Abnormalities and Genetic Counseling, 3rd edn. Oxford University Press: New York, 2004.
3. Warburton D : De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. Am J Hum Genet 1991; 49: 995–1013.
4. Rauch A, Hoyer J, Guth S et al: Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. Am J Med Genet A 2006; 140: 2063–2074.
5. Hochstenbach R, van Binsbergen E, Engelen J et al: Array analysis and karyotyping: workflow consequences based on a retrospective study of 36 325 patients with idiopathic developmental delay in the Netherlands. Eur J Med Genet 2009; 52: 161–169.
Cited by
42 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