Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Emanuela Conti

NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome

American Journal of Human Genetics
Genetics
2005English

Related publications

NF1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome

Journal of Neurology & Stroke
2017English

Neurofibromatosis-Noonan Syndrome

2020English

Molecular Genetics of Neurofibromatosis Type 1 (NF1).

Journal of Medical Genetics
Genetics
1996English

Multiple Odontogenic Cysts in a Patient With Neurofibromatosis–Noonan Syndrome

Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology
OtorhinolaryngologyOral SurgeryPathologyForensic MedicineSurgery
2016English

Neurofibromatosis Type 1 (NF1)

Atlas of Genetics and Cytogenetics in Oncology and Haematology
Cancer ResearchOncologyGeneticsHematology
2011English

Germline-Activating RRAS2 Mutations Cause Noonan Syndrome

American Journal of Human Genetics
Genetics
2019English

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity

American Journal of Human Genetics
Genetics
2002English

Noonan Syndrome: Clinical Aspects and Molecular Pathogenesis

Molecular Syndromology
Genetics
2010English

Noonan Syndrome

Paediatrica Indonesiana
2018English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy