Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants | Genetics in Medicine
Novel mutations of KRAS in patients with Noonan syndrome spectrum... | Download Scientific Diagram
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation | Genetics Research | Cambridge Core
Giant cell lesion of the jaw as a presenting feature of Noonan syndrome | BMJ Case Reports
Noonan Syndrome - Causes, Symptoms, Prognosis, Treatment
A, B : Photograph of patient 2 with definite Noonan Syndrome, 2 year-old | Download Scientific Diagram
The face of Noonan syndrome: Does phenotype predict genotype - Allanson - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library
Noonan syndrome and clinically related disorders. - Abstract - Europe PMC
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
How Dangerous Is Noonan Syndrome & Is It Contagious?
Noonan Syndrome | AAFP
Noonan Syndrome - Frequently Asked Questions / FAQs
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 ...
Noonan Syndrome | Pediatrics Clerkship | The University of Chicago | Noonan syndrome, Turner syndrome, Pediatric therapy
Facial Diagnosis Software Now A Reality! | Noonan Syndrome Awareness Association
Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations | BMC Medical Genetics | Full Text
Faces of infants with RASopathies. The panels show representative... | Download Scientific Diagram
Noonan Syndrome
NHGRI researchers and collaborators identify Noonan syndrome in diverse people
Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations | BMC Medical Genetics | Full Text
The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome | European Journal of Human Genetics
Noonan Syndrome
SciELO - Brasil - Clinical orofacial and myofunctional manifestations in an adolescent with Noonan Syndrome: a case report Clinical orofacial and myofunctional manifestations in an adolescent with Noonan Syndrome: a case report
