Suchergebnisse - "Elbracht, Miriam"

PubPharm (8)

1

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome : what has to be considered and why it is important

enthalten in: Journal of molecular medicine (Berlin, Germany) | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

2

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

enthalten in: Journal of molecular medicine | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

3

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

enthalten in: Journal of molecular medicine | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

4

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

enthalten in: Journal of molecular medicine | 2020

von Eggermann, T. | Brück, J. | Knopp, C. | +7

5

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

enthalten in: Clinical epigenetics | 2019

von Kraft, F. | Wesseler, K. | Begemann, M. | +3

6

Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

enthalten in: Clinical epigenetics | 2019

von Kraft, F. | Wesseler, K. | Begemann, M. | +3

7

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring

enthalten in: Journal of medical genetics | 2018

von Begemann, M. | Rezwan, F. | Beygo, J. | +27

8

Congenital imprinting disorders : a novel mechanism linking seemingly unrelated disorders

enthalten in: The Journal of pediatrics | 2013

von Eggermann, T. | Elbracht, M. | Schröder, C. | +4

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