Home >> Publications >> Journal >> European Journal of Human Genetics
1. Juni 2020
1. Juni 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome
Drivas TG, Li D, Nair D, Alaimo JT, Alders M, Altmuller J, Barakat TS, Bebin EM, Bertsch NL, Blackburn PR, Blesson A, Bouman AM, Brockmann K, Brunelle P, Burmeister M, Cooper GM, Denecke J, ... Wollnik B, et al.
Do you like it?
Read more

Open Positions

There are no current openings, please check back soon.

x
X
X