Different genes known to be associated with Noonan syndrome
Toward Clinical Implementation of Next-Generation Sequencing-Based Genetic Testing in Rare Diseases: Where Are We?: Trends in Genetics
Noonan Syndrome Panel – Dante Labs World
NIPT Monogenic - MGZ
Cells | Free Full-Text | Effects of Noonan Syndrome-Germline Mutations on Mitochondria and Energy Metabolism
Patient with Noonan syndrome and p.N85S mutation in KRAS gene and... | Download Scientific Diagram
Noonan Syndrome with Multiple Lentigines | Lurie Children's
Noonan syndrome - The Lancet
CleanPlex® Noonan Syndrome / RASopathies Comprehensive Panel | Paragon Genomics
Genetic Clinics
Novel mutations of KRAS in patients with Noonan syndrome spectrum... | Download Scientific Diagram
Noonan syndrome and congenital heart conditions
Cancer risk in patients with Noonan syndrome carrying a PTPN11 mutation | European Journal of Human Genetics
Novel Approach to Improve the Identification of the Bleeding Phenotype in Noonan Syndrome and Related RASopathies - The Journal of Pediatrics
Pedigree and phenotype features of the girl with Noonan Syndrome. (A)... | Download Scientific Diagram
Noonan Syndrome and RASopathies Panel
Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment - Linglart - 2020 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library
Frontiers | Genomic Diagnosis for Pediatric Disorders: Revolution and Evolution
Noonan Syndrome-Associated SHP2 Dephosphorylates GluN2B to Regulate NMDA Receptor Function - ScienceDirect
Noonan Syndrome with Multiple Lentigines - an overview | ScienceDirect Topics
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text
