Author:
Van Esch Hilde,Groenen Peter,Nesbit M. Andrew,Schuffenhauer Simone,Lichtner Peter,Vanderlinden Gert,Harding Brian,Beetz Rolf,Bilous Rudolf W.,Holdaway Ian,Shaw Nicholas J.,Fryns Jean-Pierre,Van de Ven Wim,Thakker Rajesh V.,Devriendt Koenraad
Publisher
Springer Science and Business Media LLC
Reference28 articles.
1. Daw, S. C. et al. A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Nature Genet. 13, 458– 460 (1996).
2. Schuffenhauer, S. et al. Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2). Eur. J. Hum. Genet. 6, 213–225 ( 1998).
3. Bilous, R. W. et al. Autosomal dominant familial hypoparathyroidism, sensorineural deafness, and renal dysplasia. N. Engl. J. Med. 327 , 1069–1074 (1992).
4. McKusick, V. A. Mendelian Inheritance in Man. Catalogs of Human Genes and Genetic Disorders (Johns Hopkins Univ. Press, Baltimore, 1998).
5. Van Esch, H. et al. Partial DiGeorge syndrome in two patients with a 10p rearrangement. Clin. Genet. 55, 269–276 (1999).
Cited by
494 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