Transgenic Drosophila models of Noonan syndrome causing PTPN11 gain-of-function mutations-Reference-Cited by-同舟云学术

Transgenic Drosophila models of Noonan syndrome causing PTPN11 gain-of-function mutations

Published:2006-01-06 Issue:4 Volume:15 Page:543-553
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Oishi Kimihiko,Gaengel Konstantin,Krishnamoorthy Srinivasan,Kamiya Kenichi,Kim In-Kyong,Ying Huiwen,Weber Ursula,Perkins Lizabeth A.,Tartaglia Marco,Mlodzik Marek,Pick Leslie,Gelb Bruce D.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/15/4/543/1800827/ddi471.pdf

Reference56 articles.

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2. Noonan, J.A. (1968) Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease. Am. J. Dis. Child., 116, 373–380.

3. Nora, J.J., Nora, A.H., Sinha, A.K., Spangler, R.D. and Lubs, H.A. (1974) The Ullrich–Noonan syndrome (Turner phenotype). Am. J. Dis. Child., 127, 48–55.

4. Jamieson, C.R., van der Burgt, I., Brady, A.F., van Reen, M., Elsawi, M.M., Hol, F., Jeffery, S., Patton, M.A. and Mariman, E. (1994) Mapping a gene for Noonan syndrome to the long arm of chromosome 12. Nat. Genet., 8, 357–360.

5. Marino, B., Digilio, M.C., Toscano, A., Giannotti, A. and Dallapiccola, B. (1999) Congenital heart diseases in children with Noonan syndrome: an expanded cardiac spectrum with high prevalence of atrioventricular canal. J. Pediatr., 135, 703–706.

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