PuSH - Publication Server of Helmholtz Zentrum München

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1.
Roselli, C.* et al.: Multi-ethnic genome-wide association study for atrial fibrillation. Nat. Genet. 50, 1225–1233 (2018)
2.
Stitziel, N.O.* et al.: Inactivating mutations in NPC1L1 and protection from coronary heart disease. N. Engl. J. Med. 371, 2072-2082 (2014)
3.
AMD Gene Consortium et al.: Seven new loci associated with age-related macular degeneration. Nat. Genet. 45, 433-439 (2013)
4.
Santhiya, S.T.* et al.: Molecular analysis of cataract families in India: New mutations in the CRYBB2 and GJA3 genes and rare polymorphisms. Mol. Vis. 16, 1837-1847 (2010)