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Publications by Renata Szalai
Kleefstra Syndrome in Hungarian Patients: Additional Symptoms Besides the Classic Phenotype
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
Related publications
Kleefstra Syndrome
Mutations inRIT1cause Noonan Syndrome - Additional Functional Evidence and Expanding the Clinical Phenotype
Clinical Genetics
Genetics
Classic Bartter Syndrome
Evaluation of Classic Wiskott Aldrich Syndrome With Mild Symptoms in Two Cousins: A Case Report
Iranian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Genotype-Phenotype Correlation in Brazillian Rett Syndrome Patients
Arquivos de Neuro-Psiquiatria
Biological Psychiatry
Neurology
Reversible White Matter Lesions Associated With mutantEHMT1and Kleefstra Syndrome
Neurology: Genetics
Neurology
Genetics
Metabolic Progression to Clinical Phenotype in Classic Fabry Disease
Italian Journal of Pediatrics
Child Health
Pediatrics
Perinatology
Report of Three Novel Germline CYLD Mutations in Unrelated Patients With Brooke-Spiegler Syndrome, Including Classic Phenotype, Multiple Familial Trichoepitheliomas and Malignant Transformation
Dermatology
Dermatology
HLA Class II Allele Polymorphism in Hungarian Patients With Primary Sjögren's Syndrome
Scandinavian Journal of Rheumatology
Medicine
Rheumatology
Allergy
Immunology
