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

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

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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