Author

Beatrix Elmont

Observed name: Elmont, Beatrix

OpenAlex ID: A5016113221

Case Report: Expressive Speech Disorder in a Family as a Hallmark of 7q31 Deletion Involving the FOXP2 Gene

2021 · Orsolya Nagy, Judit Kárteszi, et al. · Frontiers in Pediatrics · 6

Compound heterozygous variants in MAPK8IP3 were detected in severe congenital hypotonia mimicking lethal spinal muscular atrophy

2023 · Judit Kárteszi, Alban Ziegler, et al. · American Journal of Medical Genetics Part A · 4

Works count: 5

Citation count: 10

H-index: 2

I10-index: