Sabine Busse

Inherited cases of CNOT3‐associated intellectual developmental disorder with speech delay, autism, and dysmorphic facies

K. Zerres, T. Eggermann, I. Kurth, 2020, Clinical genetics.

Facioaudiosymphalangism syndrome and growth acceleration associated with a heterozygous NOG mutation

K. Zerres, S. Rudnik-Schöneborn, T. Eggermann, 2010, American journal of medical genetics. Part A.

Genetic (Re-)evaluation to Optimize the Care of Adults With Intellectual Disability.

I. Kurth, M. Elbracht, C. Knopp, 2022, Deutsches Arzteblatt international.

Pure distal trisomy 2q: A rare chromosomal abnormality with recognizable phenotype

K. Zerres, S. Rudnik-Schöneborn, M. Elbracht, 2009, American journal of medical genetics. Part A.