DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

References

Carta C, Pantaleoni F, Bocchinfuso G. , et al.
Germline missense mutations affecting KRAS isoform B are associated with a severe Noonan syndrome phenotype.

Am J Hum Genet 2006;
79 (01) 129-135

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