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Centre de recherche

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Régen Drouin

Formation
à venir

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Autres opportunités de carrière
Axe principal
Reproduction, santé de la mère et de l'enfant
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Regen.Drouin@crsfa.ulaval.ca

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Publications récentes (voir toutes les publications de ce chercheur)

Farmer M, Echenne B, Drouin R, Bentourkia MH. Insights in Developmental Coordination Disorder. Current pediatric reviews,  2017. Epub
Ayub S, Gadji M, Krabchi K, Cote S, Gekas J, Maranda B, Drouin R. Three new cases of terminal deletion of the long arm of chromosome 7 and literature review to correlate genotype and phenotype manifestations. American journal of medical genetics. Part A,  2016. 170A: 896-907
Dionne N, Dib S, Finsen B, Denarier E, Kuhlmann T, Drouin R, Kokoeva M, Hudson TJ, Siminovitch K, Friedman HC, Peterson AC. Functional organization of an Mbp enhancer exposes striking transcriptional regulatory diversity within myelinating glia. Glia,  2016. 64: 175-94
Emad A, Lamoureux J, Ouellet A, Drouin R. Rapid Aneuploidy Detection of Chromosomes 13, 18, 21, X and Y Using Quantitative Fluorescent Polymerase Chain Reaction with Few Microdissected Fetal Cells. Fetal diagnosis and therapy,  2015. 38: 65-76
Couture V, Drouin R, Tan SL, Moutquin JM, Bouffard C. Cross-border reprogenetic services. Clinical genetics,  2015. 87: 1-10
Drouin R, Bastien N, Millau JF, Vigneault F, Paradis I. In Cellulo DNA Analysis: LMPCR Footprinting. Methods in molecular biology (Clifton, N.J.) ,  2015. 1334: 41-84
Emad A, Bouchard EF, Lamoureux J, Ouellet A, Dutta A, Klingbeil U, Drouin R. Validation of automatic scanning of microscope slides in recovering rare cellular events: application for detection of fetal cells in maternal blood. Prenatal diagnosis,  2014. 34: 538-46
Couture V, Dubois MA, Drouin R, Moutquin JM, Bouffard C. Strengths and pitfalls of Canadian gamete and embryo donor registries: searching for beneficent solutions. Reproductive biomedicine online,  2014. 28: 369-79
Emad A, Drouin R. Evaluation of the impact of density gradient centrifugation on fetal cell loss during enrichment from maternal peripheral blood. Prenatal diagnosis,  2014. 34: 878-85
Gadji M, Crous-Tsanaclis AM, Mathieu D, Mai S, Fortin D, Drouin R. A new der(1;7)(q10;p10) leading to a singular 1p loss in a case of glioblastoma with oligodendroglioma component. Neuropathology : official journal of the Japanese Society of Neuropathology,  2014. 34: 170-8
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