Moritz Hebebrand

2PUBLICATIONS
7CO-AUTHORS
Cancer geneticsNeurogenetics
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Publications (2)

|Aug 12, 2021
BDV Syndrome: An Emerging Syndrome With Profound Obesity and Neurodevelopmental Delay Resembling Prader-Willi Syndrome.

Elisabeth Bosch, Moritz Hebebrand, Bernt Popp

|Dec 15, 2018
A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblings.

Moritz Hebebrand, Georgia Vasileiou, Mandy Krumbiegel

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