Mapping a gene for Noonan syndrome to the long arm of chromosome 12-Reference-Cited by-同舟云学术

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

Published:1994-12 Issue:4 Volume:8 Page:357-360
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Jamieson C. Ruth,van der Burgt Ineke,Brady Angela F.,van Reen Margo,Elsawi Madiha M.,Hol Frans,Jeffery Steve,Patton Michael A.,Mariman Edwin

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1294-357.pdf

Reference25 articles.

1. Noonan, J.A. & Ehmke, D.A. Associated noncardiac malformations in children with congenital heart disease. J. Paediatr. 63, 468–470 (1963).

2. Allanson, J.E. Noonan syndrome. J. med. Genet. 24, 9–13 (1987).

3. Caballin, M.R., Miro, R. & Egozcue, J. Abnormal phenotype in a child with the same balanced translocation (5;7)(p15:q22) as his father. Clin. Genet. 20, 428–431 (1981).

4. Onufer, C.N., Stephan, M.J., Thuline, H.C. & Char, F. Chromosome 13 long arm interstitial deletion associated with features of Noonan phenotype. Annal. Genetique 30, 236–239 (1993).

5. Chery, M., Philippe, C., Worms, A.M. & Gilgenkrantz, S. The Noonan syndrome. The Nancy experience revisited. Genet. Counsel. 4, 113–118 (1993).

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