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Katrine Saldern Aagaard
Katrine Saldern Aagaard
Odense University Hospital
Biology
ACVRL1
Human genetics
Hereditary haemorrhagic telangiectasia
Genetics
3
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24
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Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia.
2020
Molecular Genetics & Genomic Medicine
Katrine Saldern Aagaard
Klaus Brusgaard
Ieva Miceikaite
Martin Larsen
Anette Drøhse Kjeldsen
Emilie B. Lester
Lilian Bomme Ousager
Pernille Mathiesen Tørring
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Comorbidity among HHT patients and their controls in a 20 years follow-up period
2018
Orphanet Journal of Rare Diseases
Katrine Saldern Aagaard
Anette Drøhse Kjeldsen
Pernille Mathiesen Tørring
Anders Green
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20-year follow-up study of Danish HHT patients—survival and causes of death
2016
Orphanet Journal of Rare Diseases
Anette Drøhse Kjeldsen
Katrine Saldern Aagaard
Pernille Mathiesen Tørring
Søren Møller
Anders Green
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Citations (18)
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