Prenatal diagnosis of HNF1B ‐associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome?

Author:

Vasileiou Georgia1ORCID,Hoyer Juliane1,Thiel Christian T.1,Schaefer Jan2,Zapke Maren2,Krumbiegel Mandy1,Kraus Cornelia1,Zweier Markus3,Uebe Steffen1,Ekici Arif B.1,Schneider Michael4,Wiesener Michael5,Rauch Anita3,Faschingbauer Florian4,Reis André1,Zweier Christiane1,Popp Bernt16ORCID

Affiliation:

1. Institute of Human GeneticsFriedrich‐Alexander‐Universität Erlangen‐Nürnberg (FAU) Erlangen Germany

2. Department of Pediatrics and Adolescent MedicineUniversity Hospital of Erlangen‐Nürnberg (FAU) Erlangen Germany

3. Institute of Medical GeneticsUniversity of Zurich Schlieren‐Zurich Switzerland

4. Department of Obstetrics and GynecologyErlangen University Hospital Erlangen Germany

5. Department of Nephrology and HypertensionFriedrich‐Alexander‐Universität Erlangen‐Nürnberg (FAU) Erlangen Germany

6. Institute of Human GeneticsUniversity of Leipzig Hospitals and Clinics Leipzig Germany

Funder

Bundesministerium für Bildung und Forschung

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

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