Author:
Ruiz-Perez Victor L.,Ide Susan E.,Strom Tim M.,Lorenz Bettina,Wilson David,Woods Kathryn,King Lynn,Francomano Clair,Freisinger Peter,Spranger Stephanie,Marino Bruno,Dallapiccola Bruno,Wright Michael,Meitinger Thomas,Polymeropoulos Mihael H.,Goodship Judith
Publisher
Springer Science and Business Media LLC
Reference15 articles.
1. Ellis, R.W.B. & van Creveld, S. A syndrome characterised by ectodermal dysplasia, polydactyly, chondrodysplasia and congenital morbus cordis: report of three cases. Arch. Dis. Child. 15 , 65–84 (1940).
2. McKusick, V.A., Egeland, J.A., Eldridge, R. & Krusen, D.E. Dwarfism in the Amish I. The Ellis-van Creveld Syndrome. Bull. Johns Hopkins Hosp. 115, 306–336 (1964).
3. Polymeropoulos, M.H. et al. The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16. Genomics 35, 1– 5 (1996).
4. Howard, T.D. et al. Autosomal dominant postaxial polydactyly, nail dystrophy, and dental abnormalities map to chromosome 4p16, in the region containing the Ellis-van Creveld syndrome locus. Am. J. Hum. Genet. 61, 1405–1412 (1997).
5. Ide, S.E., Ortiz de Luna, R.I., Francomano, C.A. & Polymeropoulos, M.H. Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish. Hum. Genet. 98, 572 –575 (1996).
Cited by
284 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