Published in
Elsevier, European Journal of Medical Genetics, 12(62), p. 103587, 2019
DOI: 10.1016/j.ejmg.2018.11.021
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PUF60-SCRIB fusion transcript in a patient with 8q24.3 microdeletion and atypical Verheij syndrome
Journal article published in 2019 by
D. Abdin 
,
A. Rump,
A. Tzschach ,
K. Sarnow,
E. Schröck,
K. Hackmann,
N. Di Donato
,
A. Rump,
A. Tzschach ,
K. Sarnow,
E. Schröck,
K. Hackmann,
N. Di Donato
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