Radu Anghel Popp

2PUBLICATIONS
15CO-AUTHORS
Regenerative medicine (incl. stem cells)Neurogenetics
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Publications (2)

|May 04, 2026
Molecular Diagnosis and Phenotypic Variability of Noonan Syndrome: Experience from a Romanian Multicenter Study.

|Nov 13, 2025
Clinical and Genetic Characterization of Noonan Syndrome in a Romanian Cohort from Transylvania: Details on <i>PTPN11</i> c.922A>G Variant and Phenotypic Spectrum.

Florina Victoria Nazarie, Diana Miclea, Crina Șufană

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Frequent Collaborators

2 joint publications

Florina Victoria Nazarie

2 joint publications

Diana Miclea

2 joint publications

Ionela Maria Pascanu

2 joint publications

Camelia Alkhzouz