Author:
Barbaro Michela,Balsamo Antonio,Anderlid Britt Marie,Myhre Anne Grethe,Gennari Monia,Nicoletti Annalisa,Pittalis Maria Carla,Oscarson Mikael,Wedell Anna
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference37 articles.
1. Huret JL, Leonard C, Forestier B, Rethore MO, Lejeune J : Eleven new cases of del(9p) and features from 80 cases. J Med Genet 1988; 25: 741–749.
2. Wagstaff J, Hemann M : A familial ‘balanced’ 3;9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings. Am J Hum Genet 1995; 56: 302–309.
3. Christ LA, Crowe CA, Micale MA, Conroy JM, Schwartz S : Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome. Am J Hum Genet 1999; 65: 1387–1395.
4. Kawara H, Yamamoto T, Harada N et al: Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23. Am J Med Genet A 2006; 140: 373–377.
5. Faas BH, de Leeuw N, Mieloo H, Bruinenberg J, de Vries BB : Further refinement of the candidate region for monosomy 9p syndrome. Am J Med Genet A 2007; 143: 2353–2356.
Cited by
72 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