Franziska Schnabel
4PUBLICATIONS
1CO-AUTHORS
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Publications (4)
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|Mar 21, 2023
Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly.Franziska Schnabel, Elisabeth Schuler, Almundher Al-Maawali
|Dec 07, 2020
Aplasia cutis congenita in a CDC42-related developmental phenotype.Franziska Schnabel, Susanne B Kamphausen, Rudolf Funke
|Aug 30, 2020
Premature aging disorders: A clinical and genetic compendium.Franziska Schnabel, Uwe Kornak, Bernd Wollnik
|Jan 09, 2019
Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22.Franziska Schnabel, Mateja Smogavec, Rudolf Funke
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