Associated Papers
Common and rare variants in patients with early onset drusen maculopathy.
de Breuk A et al.
Clinical Genetics, 2022
36053979 (PubMed )
Supplement: CGE-102-414-s009.xlsx › Blad1
Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes.
Melton PE et al.
Journal of Hypertension, 2019
Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm.
Farlow JL et al.
Plos One, 2015
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