Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Léo Lavergne"'
Autor:
Léo Lavergne, Rémi Boivin, Simon Baechler, Patrick Jeuniaux, Karine Fiola, Diane Séguin, Jean-François Lefebvre, Emmanuel Milot
Publikováno v:
Forensic Science International. 331:111142
Criminal offenders missing from police files limit the capacity to reconstruct criminal networks for criminological research and operational purposes. Recent studies show that forensic DNA databanks offer potential to address this problem, through la
Publikováno v:
Forensic Science International: Genetics Supplement Series. 2:464-465
In 2000, Canada established a CODIS-based National DNA Databank (NDDB) composed of two indices: a Convicted Offender Index (COI) and a Crime Scene Index (CSI). Our laboratory populates the CSI index with single-source and mixed profiles on the 13 P+/
Autor:
Keith L. Monson, Olivier Pascal, Alan M. Giusti, Léo Lavergne, Dominique Aubert, Michèle McSween, Jean Paul Moisan, Bruce Budowle
Publikováno v:
Human heredity. 45(3)
Allele distributions were determined for several VNTR loci in the general French Caucasian population, a French regional population from Brittany and in three French Canadian populations, residing either in Montreal or in one of two other regions in
Autor:
Damian Labuda, Louis Dallaire, Daniel Sinnett, Serge B. Melançon, Michel Potier, Léo Lavergne
Publikováno v:
ResearcherID
Using human hypoxanthine-guanine phosphoribosyltransferase (HPRT) cDNA and an anonymous probe 36B-2, we examined the segregation of restriction fragment length polymorphism (RFLP) alleles with the Lesch-Nyhan phenotype in three affected families. Two
Autor:
Daniel Sinnett, S. Heuertz, Damian Labuda, Laurent Abel, Abdelaziz Sefiani, Léo Lavergne, M. C. Hors-Cayla
Publikováno v:
ResearcherID
A linkage study of eight families with incontinentia pigmenti (IP) has been performed, and linkage to site DXS52 has been established. We suggest that the IP locus lies in the Xq terminal region on the long arm of the X chromosome.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0a79e521d757f7ce1aebec44468966
https://www.ncbi.nlm.nih.gov/pubmed/2714798
https://www.ncbi.nlm.nih.gov/pubmed/2714798
Autor:
Daniel Sinnett, Louis Dallaire, Serge B Melanqon, Datnlan Labuda, Léo Lavergne, Michel Pocicr, Grant Mitchell
Publikováno v:
Pediatric Research. 21:230A-230A
IP (in McK 30830) is an inherited highly pleomorphic disease associated with central nervous system disorders in 30% of cases. It is transmitted in an X-linked dominant fashion with prenatal lethality in affected males. To date, we have used 17 probe