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No increase in female recombination frequency in the distal part of the human pseudoautosomal region.
Gilles Vergnaud
Genomics, 1994, 24 (3), pp.610-2
Journal articles
hal-01160660v1
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CEB 15 detects a VNTR locus (Het: 92%) on chromosome 1p.
V Lauthier
,
D Mariat
,
Gilles Vergnaud
Human Molecular Genetics, 1992, 1 (1), pp.63
Journal articles
hal-01160692v1
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Recent human-specific spreading of a subtelomeric domain.
S Monfouilloux
,
H Avet-Loiseau
,
V Amarger
,
I Balazs
,
C Pourcel
et al.
Journal articles
hal-01160639v1
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CEB 29 detects a VNTR locus (Het: 80%) on chromosome XY.
V Lauthier
,
J Buard
,
O Delattre
,
J Zucman
,
Gilles Vergnaud
et al.
Journal articles
istex
hal-01160691v1
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Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes.
Marie-Christine Simmler
,
François Rouyer
,
Gilles Vergnaud
,
Minna Nyström-Lahti
,
Kim Yen Ngo
et al.
Journal articles
istex
hal-01160712v1
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The EUROGEM map of human chromosome 2.
T J Flint
,
J M Hertz
,
Gilles Vergnaud
,
S Orrù
,
C B Harvey
et al.
European Journal of Human Genetics, 1993, 2 (3), pp.206-7
Journal articles
hal-01160681v1
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A DNA probe detecting multiple haplotypes of the human Y chromosome.
K y Ngo
,
Gilles Vergnaud
,
C Johnsson
,
G Lucotte
,
J Weissenbach
et al.
American Journal of Human Genetics, 1986, 38 (4), pp.407-18
Journal articles
hal-01160708v1
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A dominant modifier of transgene methylation is mapped by QTL analysis to mouse chromosome 13
Pascale Valenza-Schaerly
,
Benjamin Pickard
,
Jörn Walter
,
M Jung
,
Lucille Pourcel
et al.
Journal articles
hal-01158345v1
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Detection, cloning, and distribution of minisatellites in some mammalian genomes.
Gilles Vergnaud
,
D Gauguier
,
J J Schott
,
D Lepetit
,
V Lauthier
et al.
Journal articles
hal-01160685v1
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Use of a set of highly polymorphic minisatellite probes for the identification of cryptic 1p36.3 deletions in a large collection of patients with idiopathic mental retardation.
F Giraudeau
,
L Taine
,
V Biancalana
,
B Delobel
,
H Journel
et al.
Journal articles
hal-01158343v1
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Evaluation of a Multilocus Variable-Number Tandem-Repeat Analysis Scheme for Typing Human Brucella Isolates in a Region of Brucellosis Endemicity
M. M. Kattar
,
R. F. Jaafar
,
G. F. Araj
,
P. Le Fleche
,
G. M. Matar
et al.
Journal articles
hal-01160734v1
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Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks.
H Debrauwère
,
J Buard
,
J Tessier
,
D Aubert
,
Gilles Vergnaud
et al.
Journal articles
hal-01159817v1
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Yersinia pestis genotyping.
Gilles Vergnaud
Emerging Infectious Diseases, 2005, 11 (8), 1317-8; author reply 1318-9
Journal articles
hal-01158314v1
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Predicting human minisatellite polymorphism.
France Denoeud
,
Gilles Vergnaud
,
Gary Benson
Genome Research, 2003, 13 (5), pp.856-67
Journal articles
hal-01158326v1
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A tandem repeats database for bacterial genomes: application to the genotyping of Yersinia pestis and Bacillus anthracis.
Philippe Le Flèche
,
Yolande Hauck
,
Lucie Onteniente
,
Agnès Prieur
,
France Denoeud
et al.
Journal articles
hal-01158341v1
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Complex recombination events at the hypermutable minisatellite CEB1 (D2S90).
J Buard
,
Gilles Vergnaud
Journal articles
hal-01160661v1
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A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes.
François Rouyer
,
Marie-Christine Simmler
,
Christophe Johnsson
,
Gilles Vergnaud
,
Howard J. Cooke
et al.
Journal articles
istex
hal-01160710v1
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The EUROGEM map of human chromosome 3.
M Schürmann
,
B Müller
,
C Duvigneau
,
J Leutelt
,
S Krey
et al.
European Journal of Human Genetics, 1993, 2 (3), pp.208-9
Journal articles
hal-01160680v1
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The EUROGEM map of human chromosome 17.
S A Cox
,
Gilles Vergnaud
,
J Milan
,
F Moreno
,
J Beckmann
et al.
European Journal of Human Genetics, 1993, 2 (3), pp.236-7
Journal articles
hal-01160665v1
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High resolution, on-line identification of strains from the Mycobacterium tuberculosis complex based on tandem repeat typing.
Philippe Le Flèche
,
Michel Fabre
,
France Denoeud
,
Jean-Louis Koeck
,
Gilles Vergnaud
et al.
Journal articles
hal-01158328v1
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The EUROGEM map of human chromosome 15.
C Joyce
,
L Fanning
,
S Malcolm
,
I Richard
,
O Broux
et al.
European Journal of Human Genetics, 1993, 2 (3), pp.232-3
Journal articles
hal-01160667v1
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CRISPR elements in Yersinia pestis acquire new repeats by preferential uptake of bacteriophage DNA, and provide additional tools for evolutionary studies.
C Pourcel
,
G Salvignol
,
Gilles Vergnaud
Journal articles
hal-01158317v1
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[Structure and evolution of human sub-telomeric regions].
Gilles Vergnaud
Journal de la Société de Biologie, 1998, 193 (1), pp.35-40
Journal articles
hal-01159815v1
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Report of the second international workshop on human chromosome 5 mapping: consensus genetic map.
R Plaetke
,
J Weber
,
S Wood
,
M Dean
,
a J Jeffreys
et al.
Cytogenetics and Cell Genetics, 1991, 61 (4), pp.237-42
Journal articles
hal-01160695v1
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A synthetic probe, STR 14C13, detects a new polymorphic locus on chromosome arm 7q (D7S450).
V Lauthier
,
D Mariat
,
M Zoroastro
,
Gilles Vergnaud
Nucleic Acids Research, 1991, 19 (14), pp.4014
Journal articles
hal-01160700v1
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The EUROGEM map of human chromosome 1.
R Kumar-Singh
,
Hui Wang
,
B Carritt
,
T A Kruse
,
T V Mccarthy
et al.
European Journal of Human Genetics, 1993, 2 (3), pp.204-205
Journal articles
hal-01160682v1
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Generation of a CRISPR database for Yersinia pseudotuberculosis complex and role of CRISPR-based immunity in conjugation.
Katja A Koskela
,
Laura Mattinen
,
Laura Kalin-Mänttäri
,
Gilles Vergnaud
,
Olivier Gorgé
et al.
Journal articles
istex
hal-01152593v1
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Tandem repeats analysis for the high resolution phylogenetic analysis of Yersinia pestis
Christine Pourcel
,
Flore André-Mazeaud
,
Heinrich Neubauer
,
Françoise Ramisse
,
Gilles Vergnaud
et al.
Journal articles
hal-01158319v1
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Minisatellite polymorphism as a tool to distinguish closely related Lactococcus lactis strains.
Pascal Quénée
,
Elodie Lepage
,
Woojin Scott Kim
,
Gilles Vergnaud
,
Alexandra Gruss
et al.
Journal articles
hal-01158315v1
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A polymorphic porcine dinucleotide repeat S0559 (BHT0107) at chromosome 6q28-q31.
B Høyheim
,
V Amarger
,
Gilles Vergnaud
,
P D Thomsen
Animal Genetics, 1998, 29 (6), pp.460
Journal articles
hal-01160636v1
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