Alrun Hotz
11PUBLICATIONS
15CO-AUTHORS
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Publications (11)
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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
|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
|Aug 27, 2021
Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome.Julia Kopp, Cristina Has, Alrun Hotz
|Jan 13, 2021
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients.Alrun Hotz, Julia Kopp, Emmanuelle Bourrat
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Frequent Collaborators
10 joint publications
Judith Fischer
5 joint publications
Andreas D Zimmer
4 joint publications
Katalin Komlosi
3 joint publications
Svenja Alter
2 joint publications
Lisa Heinz
2 joint publications
Regina C Betz
1 joint publications
Nataliya Di Donato
1 joint publications
Andreas Tzschach
1 joint publications
Nadja Ballin
1 joint publications
Cristina Has
