Svenja Rademacher
6PUBLICATIONS
10CO-AUTHORS

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Publications (6)
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|Mar 28, 2024
Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations.Alrun Hotz, Regina Fölster-Holst, Vinzenz Oji
|Mar 29, 2023
Mutational Spectrum of the ABCA12 Gene and Genotype-Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis.Alrun Hotz, Julia Kopp, Emmanuelle Bourrat
|Jan 23, 2023
Adding up the desmosomal genes causing syndromes with hair and skin involvement: identification of TUFT1 by state-of-the-art whole-genome sequencing.Judith Fischer, Svenja Alter
|Mar 25, 2022
First Description of Inheritance of a Postzygotic OPA1 Mosaic Variant.Svenja Alter, Navid Farassat, Sebastian Küchlin
|Oct 23, 2021
The Importance of Extended Analysis Using Current Molecular Genetic Methods Based on the Example of a Cohort of 228 Patients with Hereditary Breast and Ovarian Cancer Syndrome.Luise D Resch, Alrun Hotz, Andreas D Zimmer
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Frequent Collaborators
5 joint publications
Judith Fischer
3 joint publications
Alrun Hotz
3 joint publications
Katalin Komlosi
2 joint publications
Andreas D Zimmer
1 joint publications
Navid Farassat
1 joint publications
Sebastian Küchlin
1 joint publications
Regina C Betz
1 joint publications
Dora V Stölzl
1 joint publications
Jorge Frank
1 joint publications
Lotta Wankner