Hans Christian Laugaard-Jacobsen

Research activity per year

2017
De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome
Lundsgaard, M., Le, V. Q., Ernst, A., Laugaard-Jacobsen, H. C., Rasmussen, K., Pedersen, I. S. & Petersen, M. B., 2017, In: Molecular Syndromology. 8, 1, p. 24-29 6 p.
Research output: Contribution to journal › Journal article › Research › peer-review
7 Citations (Scopus)
Muscular response to the first three months of deflazacort treatment in boys with Duchenne muscular dystrophy
Jensen, L., Petersson, S. J., Illum, N. O., Laugaard-Jacobsen, H. C., Thelle, T. H., Jørgensen, L. H. & Schrøder, H. D., 2017, In: Journal of Musculoskeletal and Neuronal Interactions. 17, 2, p. 8-18 11 p.
Research output: Contribution to journal › Journal article › Research › peer-review

Open Access
5 Citations (Scopus)

Research output