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Article

A PTPN11 gene mutation (Y63C) causing Noonan syndrome is not associated with short stature in general population.

The Tohoku journal of experimental medicine - 1 Mar 2006

Takahashi Ikuko, Utsunomiya Maki, Inoue Kayoko, Takahashi Tsutomu, Nozaki Jun-Ichi, Wada Yasuhiko, Takada Goro, Koizumi Akio

Abstract excerpt

Human growth is a highly complicated process, but it is obviously influenced by a genetic factor. Recent genome-wide linkage analyses suggested some genetic regions underlying stature variations. However, any specific genes underlying stature variations have not been identified. Noonan syndrome (NS) is an autosomal dominant disorder clinically characterized by short stature, minor facial anomalies, and congenital...

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Identifiers

PMID: 16498234
DOI: 10.1620/tjem.208.255

Genes

PTPN11

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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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A PTPN11 gene mutation (Y63C) causing Noonan syndrome is not associated with short stature in general population.PMID 16498234Read ↗

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