C. Schröder

Translocation and Deletion around SOX9 in a Patient with Acampomelic Campomelic Dysplasia and Sex Reversal

R. Ullmann, P. Wieacker, M. Volleth, 2010, Sexual Development.

Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)

P. Bauer, L. Schöls, E. Leshinsky‐Silver, 2012, neurogenetics.

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

T. Fehm, M. Golatta, C. Engel, 2023, Breast Care.

Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47)

P. Bauer, L. Schöls, E. Leshinsky‐Silver, 2012, neurogenetics.