15 results on '"Génin, Emmanuelle"'
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2. Human genetic structure in Northwest France provides new insights into West European historical demography
3. Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants
4. How local reference panels improve imputation in French populations
5. Heritability: What's the point? What is it not for? A human genetics perspective
6. Expanding ACMG variant classification guidelines into a general framework
7. Rare variant association testing in the non-coding genome
8. The genetic history of France
9. Missing heritability of complex diseases: case solved?
10. Association of modifiers and other genetic factors explain Marfan syndrome clinical variability
11. Estimating the age of p.(Phe508del) with family studies of geographically distinct European populations and the early spread of cystic fibrosis
12. Correction: The genetic history of France
13. Identifying modifier genes of monogenic disease: strategies and difficulties
14. Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity
15. Detection of polymorphism in the RING3 gene by high-throughput fluorescent SSCP analysis
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