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You searched for: Author/Creator Devriendt, KLimit your search
- Devriendt, K [remove] 25
- 616.042 25
- Medical genetics -- Periodicals 25
- 22q11.2 deletion -- linkage disequilibrium block structure -- TBX1 -- congenital heart defect 1
- 4p deletion syndrome -- array CGH -- olfactory receptor gene cluster -- WHSC1 -- Wolf-Hirschhorn syndrome 1
- AV, atrioventricular -- DHPLC, denaturing high performance liquid chromatography -- EPS, electrophysiological study -- ES, extra-stimuli -- ICCD, isolated cardiac conduction defect -- PES, programmed electrical stimulation -- SNPs, single nucleotide polymorphisms -- WT, wildtype 1
- BAC, bacterial artificial chromosome -- CGH, comparative genomic hybridisation -- CNV, copy number variation -- MCA/MR, mental retardation and multiple congenital anomalies -- PAC, P1 derived artificial chromosome -- RTQ-PCR, real time quantitative polymerase chain reaction 1
- Brugada syndrome -- conduction disease -- gene regulation -- ion channels -- splice mutations 1
- CHD, congenital heart disease -- DGS, DiGeorge syndrome -- SNP, single nucleotide polymorphism -- TDT, transmission disequilibrium test -- TGA, transposition of the great arteries -- TOF, tetralogy of Fallot -- VEGF, vascular endothelial growth factor -- VSD, ventricular septum defect 1
- DGS/VCFS, DiGeorge or velocardiofacial syndrome -- GOLD, graphical package for overview of linkage disequilibrium -- LD, linkage disequilibrium -- PHASE, software package for phylogenetics and sequence evolution -- SNP, single nucleotide polymorphism 1
- SHFM3 -- 10q24 microduplication -- distal limb deficiencies with micrognathia syndrome -- ectrodactyly -- reduction limb defects -- genetics -- clinical genetics -- cytogenetics -- genetic screening/counselling -- molecular genetics 1