Information till studenter och medarbetare med anledning av covid-19 (Uppdaterad: 14 januari 2021)

English
Umeå universitet
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Magnus Burstedt

Kontakt

E-post
magnus.burstedt@umu.se

Verksam vid

Anknytning
Anknuten som överläkare till Institutionen för medicinsk biovetenskap
Plats
By 6M, Sjukhusområdet Umeå universitet, 901 85 Umeå
2020
Pre- and postnatal growth failure with microcephaly due to two novel heterozygous IGF1R mutations and response to growth hormone treatment
Acta Paediatrica, John Wiley & Sons 2020, Vol. 109, (10)
Gkourogianni, Alexandra; Andrade, Anenisia C.; Jonsson, Björn-Anders; et al.
2018
Genomic screening in rare disorders: new mutations and phenotypes, highlighting ALG14 as a novel cause of severe intellectual disability
Clinical Genetics, John Wiley & Sons 2018, Vol. 94, (6) : 528-537
Kvarnung, Malin; Taylan, Fulya; Nilsson, Daniel; et al.
2013
Genotype-phenotype correlations in Bothnia dystrophy caused by RLBP1 gene sequence variations
Acta Ophthalmologica, Vol. 91, (5) : 437-444
Burstedt, Marie; Jonsson, Frida; Köhn, Linda; et al.
Visa publikationer i DiVA