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- Lyonnet, S [remove] 31
- Medical genetics -- Periodicals 28
- 616.042 26
- 616.0420 2
- 616.12 2
- Cardiology -- Periodicals 2
- Heart -- Diseases -- Treatment -- Periodicals 2
- 22q deletion -- tetralogy of Fallot -- congenital heart disease 1
- 618.920005 1
- 95% CI, 95% confidence interval -- HSCR, Hirschsprung disease -- IBD1, one allele identical by descent -- OR, odds ratio -- SNP, single nucleotide polymorphism -- TDT, transmission disequilibrium test 1
- CCHS, congenital central hypoventilation syndrome -- HSCR, Hirschsprung's disease -- MWS, Mowat-Wilson syndrome -- SNP, single nucleotide polymorphism 1