Ghent University Academic Bibliography

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- Miscellaneous
Genetic testing in patients with congenital heart disease : you do no harm when using the right tools!

Julie De Backer (UGent) and Laura Muiño Mosquera (UGent)

(2023) CIRCULATION-GENOMIC AND PRECISION MEDICINE. 16(2).
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- Journal Article
- A1
- open access
Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline

Laura Muiño Mosquera (UGent) , Felke Steijns, Tjorven Audenaert (UGent) , Ilse Meerschaut, Anne De Paepe (UGent) , Wouter Steyaert (UGent) , Sofie Symoens (UGent) , Paul Coucke (UGent) , Bert Callewaert (UGent) , Marjolijn Renard (UGent) , et al.

(2018) CIRCULATION-GENOMIC AND PRECISION MEDICINE. 11.
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Cardiovascular health in Turner syndrome : a scientific statement from the American Heart Association

Michael Silberbach, Jolien W Roos-Hesselink, Niels H Andersen, Alan C Braverman, Nicole Brown, R Thomas Collins, Julie De Backer (UGent) , Kim A Eagle, Loren F Hiratzka, Walter H, Jr Johnson, et al.

(2018) CIRCULATION-GENOMIC AND PRECISION MEDICINE. 11(10).
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- Miscellaneous
Looking for the missing links : challenges in the search for genotype-phenotype correlation in Marfan syndrome

Julie De Backer (UGent) , Laurence Campens (UGent) and Laura Muiño Mosquera (UGent)

(2018) CIRCULATION-GENOMIC AND PRECISION MEDICINE. 11.

Academic Bibliography

Genetic testing in patients with congenital heart disease : you do no harm when using the right tools!

Tailoring the American College of Medical Genetics and Genomics and the Association for Molecular Pathology guidelines for the interpretation of sequenced variants in the FBN1 gene for Marfan syndrome : proposal for a disease- and gene-specific guideline

Cardiovascular health in Turner syndrome : a scientific statement from the American Heart Association

Looking for the missing links : challenges in the search for genotype-phenotype correlation in Marfan syndrome

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