Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype

Author:

Tedesco Maria Giovanna12,Lonardo Fortunato3,Ceccarini Caterina4,Cesarano Carla4,Digilio Maria Cristina5,Magliozzi Monia5,Rogaia Daniela1,Mencarelli Amedea1,Leoni Chiara6ORCID,Piscopo Carmelo7,Imperatore Valentina1ORCID,Falco Maria Teresa3ORCID,Fontana Paolo3ORCID,Nardone Anna Maria8,Novelli Antonio5,Troiani Stefania19,Seri Marco10,Prontera Paolo1ORCID

Affiliation:

1. Medical Genetics Unit Santa Maria della Misericordia Hospital and University of Perugia Perugia Italy

2. Genetics Unit "Mauro Baschirotto" Institute for Rare Diseases (B.I.R.D.) Vicenza Italy

3. Medical Genetics Unit "San Pio" Hospital Benevento Italy

4. Cytogenetics Unit Policlinico Riuniti, University Hospitals Foggia Foggia Italy

5. Laboratory of Medical Genetics, Medical Genetics Bambino Gesù Children's Hospital, IRCCS Rome Italy

6. Department of Woman and Child Health and Public Health Center for Rare Diseases and Birth Defects, Fondazione Policlinico Universitario A. Gemelli IRCCS Rome Italy

7. U.O.S.C. Medical Genetics, A.O.R.N. "A. Cardarelli" Naples Italy

8. Medical Genetics Laboratory "Policlinico Tor Vergata" Hospital Rome Italy

9. Division of Neonatology and Neonatal Intensive Care Unit Santa Maria della Misericordia Hospital of Perugia Perugia Italy

10. Medical Genetics Unit Policlinico S. Orsola‐Malpighi, University of Bologna Bologna Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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