Hermine E Veenstra-Knol
2PUBLICATIONS
5CO-AUTHORS

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Publications (2)
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|Jul 22, 2025
Expanding the Clinical Spectrum of Cousin Syndrome: A Novel Biallelic Missense Variant in TBX15 Causing a Milder Phenotype.Suzanne E L Detiger, Martijn V Verhagen, Tuula Rinne
|Jun 09, 2023
Expanding the phenotype of anauxetic dysplasia caused by biallelic NEPRO mutations: A case report.P Christian Remmelzwaal, Martijn V Verhagen, Jan D H Jongbloed
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