Report for Langlois S

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References (6)

Title : Guideline No. 410: Prevention, Screening, Diagnosis, and Pregnancy Management for Fetal Neural Tube Defects - Douglas_2020_J.Obstet.Gynaecol.Can_43_124
Author(s) : Douglas Wilson R , Van Mieghem T , Langlois S , Church P
Ref : J Obstet Gynaecol Can , 43 :124 , 2020
Abstract : Douglas_2020_J.Obstet.Gynaecol.Can_43_124
ESTHER : Douglas_2020_J.Obstet.Gynaecol.Can_43_124
PubMedSearch : Douglas_2020_J.Obstet.Gynaecol.Can_43_124
PubMedID: 33212246

Title : Prenatal screening, diagnosis, and pregnancy management of fetal neural tube defects - Wilson_2014_J.Obstet.Gynaecol.Can_36_927
Author(s) : Wilson RD , Audibert F , Brock JA , Campagnolo C , Carroll J , Cartier L , Chitayat D , Gagnon A , Johnson JA , Langlois S , MacDonald WK , Murphy-Kaulbeck L , Okun N , Pastuck M , Popa V
Ref : J Obstet Gynaecol Can , 36 :927 , 2014
Abstract : Wilson_2014_J.Obstet.Gynaecol.Can_36_927
ESTHER : Wilson_2014_J.Obstet.Gynaecol.Can_36_927
PubMedSearch : Wilson_2014_J.Obstet.Gynaecol.Can_36_927
PubMedID: 25375307

Title : Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency - Benlian_1996_Am.J.Hum.Genet_59_431
Author(s) : Benlian P , Foubert L , Gagne E , Bernard L , De Gennes JL , Langlois S , Robinson W , Hayden M
Ref : American Journal of Human Genetics , 59 :431 , 1996
Abstract : Benlian_1996_Am.J.Hum.Genet_59_431
ESTHER : Benlian_1996_Am.J.Hum.Genet_59_431
PubMedSearch : Benlian_1996_Am.J.Hum.Genet_59_431
PubMedID: 8755931
Gene_locus related to this paper: human-LPL

Title : A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency - Langlois_1989_Proc.Natl.Acad.Sci.U.S.A_86_948
Author(s) : Langlois S , Deeb S , Brunzell JD , Kastelein JJ , Hayden MR
Ref : Proc Natl Acad Sci U S A , 86 :948 , 1989
Abstract : Langlois_1989_Proc.Natl.Acad.Sci.U.S.A_86_948
ESTHER : Langlois_1989_Proc.Natl.Acad.Sci.U.S.A_86_948
PubMedSearch : Langlois_1989_Proc.Natl.Acad.Sci.U.S.A_86_948
PubMedID: 2536938

Title : Characterization of six partial deletions in the low-density-lipoprotein (LDL) receptor gene causing familial hypercholesterolemia (FH) - Langlois_1988_Am.J.Hum.Genet_43_60
Author(s) : Langlois S , Deeb S , Brunzell J , Kastelein JJ , Hayden MR
Ref : American Journal of Human Genetics , 43 :60 , 1988
Abstract : Langlois_1988_Am.J.Hum.Genet_43_60
ESTHER : Langlois_1988_Am.J.Hum.Genet_43_60
PubMedSearch : Langlois_1988_Am.J.Hum.Genet_43_60
PubMedID: 2837085

Title : A unique insertion accounts for a significant proportion of the mutations in the lipoprotein lipase (LPL) gene. (Abstract) - Langlois_1988_Am.J.Hum.Genet_43_A191
Author(s) : Langlois S , Deeb S , Brunzell J , Kastelein JJ , Hayden MR
Ref : American Journal of Human Genetics , 43 :A191 , 1988
Abstract : Langlois_1988_Am.J.Hum.Genet_43_A191
ESTHER : Langlois_1988_Am.J.Hum.Genet_43_A191
PubMedSearch : Langlois_1988_Am.J.Hum.Genet_43_A191
PubMedID: