Does the Rare A172G Mutation of PTPN11 Gene Convey a Mild Noonan Syndrome Phenotype? | Citedby Results | Hormone Research in Paediatrics | Karger Publishers

Skip to Main Content

Skip Nav Destination

Does the Rare A172G Mutation of PTPN11 Gene Convey a Mild Noonan Syndrome Phenotype?

Hormone Research (2006) 66 (3): 124–131.

This article has been cited by the following articles in journals that are participating in CrossRef Cited-by Linking.

BRAF gene: From human cancers to developmental syndromes

Muhammad Ramzan Manwar Hussain
Mukhtiar Baig
Hussein Sheik Ali Mohamoud
Zaheer Ulhaq
Daniel C. Hoessli
Ghaidaa Siraj Khogeer
Ranem Radwan Al-Sayed
Jumana Yousuf Al-Aama

Saudi Journal of Biological Sciences (2015) 22 (4): 359.

Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment

Anna Papadopoulou
Michalis Issakidis
Evangelia Gole
Konstantina Kosma
Helen Fryssira
Andreas Fretzayas
Polyxeni Nicolaidou
Sophia Kitsiou-Tzeli

European Journal of Pediatrics (2012) 171 (1): 51.

A novel HRAS substitution (c.266C>G; p.S89C) resulting in decreased downstream signaling suggests a new dimension of RAS pathway dysregulation in human development

Karen W. Gripp
Eugenia Bifeld
Deborah L. Stabley
Elizabeth Hopkins
Stefanie Meien
Kathy Vinette
Katia Sol‐Church
Georg Rosenberger

American Journal of Medical Genetics Part A (2012) 158A (9): 2106.

Comprehensive genetic analysis of overlapping syndromes of RAS/RAF/MEK/ERK pathway

Munkhtuya Tumurkhuu
Makiko Saitoh
Atsushi Sato
Kan Takahashi
Masakazu Mimaki
Junko Takita
Kazuhide Takeshita
Takehiro Hama
Akira Oka
Masashi Mizuguchi

Pediatrics International (2010) 52 (4): 557.

Analysis of the PTPN11 gene in idiopathic short stature children and Noonan syndrome patients

Lize V. Ferreira
Silvia C. A. L. Souza
Luciana R. Montenegro
Alexsandra C. Malaquias
Ivo J. P. Arnhold
Berenice B. Mendonca
Alexander A. L. Jorge

Clinical Endocrinology (2008) 69 (3): 426.