S.B. Melançon

Prenatal diagnosis of hereditary tyrosinaemia: Measurement of succinylacetone in amniotic fluid

R. Gagné, A. Lescault, A Grenier et al. · Prenatal Diagnosis · 1982 · 46 citations

Medicine, Genetics, Obstetrics +6

Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: Their characterization and delineation of defects in pregnancies at risk

Louis Dallaire, Jacques L. Michaud, S.B. Melançon et al. · Prenatal Diagnosis · 1991 · 43 citations

Medicine, Genetics, Obstetrics +17

Prenatal diagnosis of smith–lemli–opitz syndrome is possible by measurement of 7‐dehydrocholesterol in amniotic fluid

Louis Dallaire, G. H. Mitchell, Robert Giguère et al. · Prenatal Diagnosis · 1995 · 31 citations

Medicine, Endocrinology, Obstetrics +16

Molecular analyses of a Lesch-Nyhan syndrome mutation (hprt Montreal) by use of T-lymphocyte cultures

T R Skopek, Leslie Recio, Deborah Simpson et al. · Human Genetics · 1990 · 25 citations

Life Sciences, Genetics, Molecular Genetics +12

Short communications prenatal detection of the autosomal recessive type of polycystic kidney disease by trehalase assay in amniotic fluid

P Morin, Louis Dallaire, S.B. Melançon et al. · Prenatal Diagnosis · 1981 · 25 citations

Medicine, Nephrology, Obstetrics +14