Tina Duelund Hjortshøj

Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care

Ivanovski, I., Djuric, O., Caraffi, S. G., Santodirocco, D., Pollazzon, M., Rosato, S., Cordelli, D. M., Abdalla, E., Accorsi, P., Adam, M. P., Ajmone, P. F., Badura-Stronka, M., Baldo, C., Baldi, M., Bayat, A., Bigoni, S., Bonvicini, F., Breckpot, J., Callewaert, B., Cocchi, G. & 30 others, Cuturilo, G., De Brasi, D., Devriendt, K., Dinulos, M. B., Hjortshøj, Tina Duelund, Epifanio, R., Faravelli, F., Fiumara, A., Formisano, D., Giordano, L., Grasso, M., Grønborg, S., Iodice, A., Iughetti, L., Kuburovic, V., Kutkowska-Kazmierczak, A., Lacombe, D., Lo Rizzo, C., Luchetti, A., Malbora, B., Mammi, I., Mari, F., Montorsi, G., Moutton, S., Møller, R. S., Muschke, P., Nielsen, Jens Erik Klint, Obersztyn, E., Pantaleoni, C. & Pellicciari, A., 1 Sep 2018, In: Genetics in Medicine. 20, 9, p. 965-975 11 p.

Research output: Contribution to journal › Journal article › Research › peer-review

The first Danish patient with a recognisable genetic KBG syndrome

Bayat, Allan, Møller, L. B. & Hjortshøj, Tina Duelund, 12 Mar 2018, In: Ugeskrift for Laeger. 180, 11

Research output: Contribution to journal › Journal article › Research › peer-review