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You searched for: Author/Creator Lascorz, J- Lascorz, J [remove] 5
- 616.042 3
- Medical genetics -- Periodicals 3
- 616.723005 2
- Rheumatism -- Periodicals 2
- 22q11.2 atypical deletions -- affected sib pair -- congenital heart defects -- mental retardation -- choanal atresia 1
- CARD15 -- PSORS1 -- psoriatic arthritis -- genetic association 1
- HCR, Hox control region -- SNP, single nucleotide polymorphism 1
- association -- linkage disequilibrium -- psoriasis -- R620W 1
- ctCHD, conotruncal congenital heart defects -- DGS, DiGeorge syndrome -- FISH, fluorescent in situ hybridisation -- LCR, low copy repeat -- MR/MCA, mental retardation/multiple congenital anomalies -- PDA, persistent ductus arteriosis Botalli -- PFO, persistent foramen ovale -- SNP, single nucleotide polymorphism -- VCFS, velocardiofacial syndrome -- VSD, ventricular septal defect 1
- htSNP, haplotype tag SNP -- LD, linkage disequilibrium -- SNP, single nucleotide polymorphism 1