SciELO - Brasil - 1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to <i>NRAS</i> gene haploinsufficiency 1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to <i>NRAS</i> gene ...
Syndromes - The RASopathies Network
Noonan Syndrome | Obgyn Key
Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations | BMC Medical Genetics | Full Text
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation | Genetics Research | Cambridge Core
Frontiers | Automated Facial Recognition for Noonan Syndrome Using Novel Deep Convolutional Neural Network With Additive Angular Margin Loss
A, B : Photograph of patient 2 with definite Noonan Syndrome, 2 year-old | Download Scientific Diagram
Novel mutations of KRAS in patients with Noonan syndrome spectrum... | Download Scientific Diagram
Noonan Syndrome | Pediatrics Clerkship | The University of Chicago | Noonan syndrome, Turner syndrome, Pediatric therapy
Noonan Syndrome
Noonan Syndrome | AAFP
Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations | BMC Medical Genetics | Full Text
Mutation and Phenotypic Spectrum of Patients With RASopathies
Noonan syndrome: improving recognition and diagnosis | Archives of Disease in Childhood
Diagnosis by Facial Analysis – An Exciting Advance for Noonan Syndrome | Noonan Syndrome Awareness Association
Noonan Syndrome - Frequently Asked Questions / FAQs
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation | Genetics in Medicine
The face of Noonan syndrome: Does phenotype predict genotype - Allanson - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Giant cell lesion of the jaw as a presenting feature of Noonan syndrome | BMJ Case Reports
NHGRI researchers and collaborators identify Noonan syndrome in diverse people
Dental and maxillofacial features of Noonan Syndrome: Case series of ten patients - ScienceDirect
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants | Genetics in Medicine
Noonan syndrome - The Lancet
