All papers authored by Andreas Hahn
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2023
Alexander H. Swan 
,
Roland F. R. Schindler ,
Marco Savarese ,
Isabelle Mayer,
Susanne Rinné ,
Felix Bleser,
Anne Schänzer ,
Andreas Hahn ,
Mario Sabatelli ,
Francesco Perna ,
Kathryn Chapman,
Mark Pfuhl ,
Alan C. Spivey ,
Niels Decher ,
Bjarne Udd
and 2 other authors
Download from doi.org
,
Roland F. R. Schindler ,
Marco Savarese ,
Isabelle Mayer,
Susanne Rinné ,
Felix Bleser,
Anne Schänzer ,
Andreas Hahn ,
Mario Sabatelli ,
Francesco Perna ,
Kathryn Chapman,
Mark Pfuhl ,
Alan C. Spivey ,
Niels Decher ,
Bjarne Udd
and 2 other authors
Download from doi.org
Alexander H. Swan ,
Roland F. R. Schindler ,
Marco Savarese ,
Isabelle Mayer,
Susanne Rinné ,
Felix Bleser,
Anne Schänzer ,
Andreas Hahn ,
Mario Sabatelli ,
Francesco Perna ,
Kathryn Chapman,
Mark Pfuhl ,
Alan C. Spivey ,
Niels Decher ,
Bjarne Udd
and 2 other authors
Download from doi.org
,
Roland F. R. Schindler ,
Marco Savarese ,
Isabelle Mayer,
Susanne Rinné ,
Felix Bleser,
Anne Schänzer ,
Andreas Hahn ,
Mario Sabatelli ,
Francesco Perna ,
Kathryn Chapman,
Mark Pfuhl ,
Alan C. Spivey ,
Niels Decher ,
Bjarne Udd
and 2 other authors
Download from doi.org
2021
Schanzer A.,
Anne Schänzer ,
Melanie T. Achleitner,
Achleitner Mt,
Dietrich Trümbach ,
Trumbach D.,
Laurence Hubert ,
Hubert L.,
Arnold Munnich ,
Munnich A.,
Barbara Ahlemeyer,
Saskia B. Wortmann,
Maha M. AlAbdulrahim,
Ahlemeyer B.,
Philipp A. Greif
and 47 other authors
,
Melanie T. Achleitner,
Achleitner Mt,
Dietrich Trümbach ,
Trumbach D.,
Laurence Hubert ,
Hubert L.,
Arnold Munnich ,
Munnich A.,
Barbara Ahlemeyer,
Saskia B. Wortmann,
Maha M. AlAbdulrahim,
Ahlemeyer B.,
Philipp A. Greif
and 47 other authors
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism
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2016
Karim Kouz,
Christina Lissewski ,
Stephanie Spranger,
Diana Mitter,
Angelika Riess,
Vanesa Lopez-Gonzalez,
Sabine Lüttgen,
Hatip Aydin ,
Florian von Deimling,
Christina Evers,
Andreas Hahn ,
Maja Hempel,
Ulrike Issa,
Anne-Karin Kahlert ,
Adrian Lieb
and 11 other authors
,
Stephanie Spranger,
Diana Mitter,
Angelika Riess,
Vanesa Lopez-Gonzalez,
Sabine Lüttgen,
Hatip Aydin ,
Florian von Deimling,
Christina Evers,
Andreas Hahn ,
Maja Hempel,
Ulrike Issa,
Anne-Karin Kahlert ,
Adrian Lieb
and 11 other authors
Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
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