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Publications by Éva Erhardt

A Unique Haplotype of RCCX Copy Number Variation: From the Clinics of Congenital Adrenal Hyperplasia to Evolutionary Genetics

European Journal of Human Genetics
Genetics
2017English

The Importance of the Multiplex Ligation-Dependent Probe Amplification in the Identification of a Novel Two-Exon Deletion of the NR5A1 Gene in a Patient With 46,XY Differences of Sex Development

Molecular Biology Reports
MedicineGeneticsMolecular Biology
2019English

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