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Article

Genotype differences in cognitive functioning in Noonan syndrome.

Genes, brain, and behavior - 1 Apr 2009

Pierpont E I, Pierpont M E, Mendelsohn N J, Roberts A E, Tworog-Dube E, Seidenberg M S

Abstract excerpt

Noonan syndrome (NS) is an autosomal-dominant genetic disorder associated with highly variable features, including heart disease, short stature, minor facial anomalies and learning disabilities. Recent gene discoveries have laid the groundwork for exploring whether variability in the NS phenotype is related to differences at the genetic level. In this study, we examine the influence of both genotype and...

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Source

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Identifiers

PMID: 19077116
DOI: 10.1111/j.1601-183X.2008.00469.x
PMCID: PMC2760992

Genes

PTPN11
SOS1
BRAF

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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