HSPA6
            : A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum

Kause, Franziska ORCID Institute of Human Genetics, University of Bonn Bonn Germany
Zhang, Rong Department of GenomicsLife & Brain Center Bonn Germany
Ludwig, Michael Department of Clinical Chemistry and Clinical PharmacologyUniversity of Bonn Bonn Germany
Schmiedeke, Eberhard Clinic for Paediatric Surgery and Paediatric UrologyKlinikum Bremen‐Mitte Bremen Germany
Rissmann, Anke Malformation Monitoring Centre Saxony‐Anhalt, Medical FacultyOtto‐von‐Guericke University Magdeburg Germany
Thiele, Holger Cologne Center for GenomicsUniversity of Cologne Cologne Germany
Altmueller, Janine Center for Molecular Medicine Cologne (CMMC)University of Cologne Cologne Germany
Herms, Stefan Department of Biomedicine, Human Genomics Research GroupUniversity of Basel Basel Switzerland
Hilger, Alina C. Children's HospitalUniversity of Bonn Bonn Germany
Hildebrandt, Friedhelm Division of NephrologyBoston Children's Hospital, HMS Boston Massachusetts
Reutter, Heiko ORCID Department of Neonatology and Pediatric Intensive CareChildren's Hospital, University of Bonn Bonn Germany