论文信息 - Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation - 字舞流文

Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation

Debopam Samanta

[1] J. Allanson,et al. Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines , 2010, Pediatrics.

[2] Mark S. Seidenberg,et al. Genotype differences in cognitive functioning in Noonan syndrome , 2009, Genes, brain, and behavior.

[3] Wendy Schackwitz,et al. Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome , 2006, Nature Genetics.

[4] M. Burch,et al. A clinical study of Noonan syndrome. , 1992, Archives of disease in childhood.