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3. FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

4. A genome-wide search for new imprinted genes in the human placenta identifies DSCAM as the first imprinted gene on chromosome 21

6. Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

8. Polymorphisms in 33 inflammatory genes and risk of myocardial infarction—a system genetics approach

10. The human T locus and spina bifida risk

12. sY116, a human Y-linked polymorphic STS

13. Donor splice-site mutations in WT1 are responsible for Frasier syndrome

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