The Endogenous Retroviral Locus ERVWE1 Is a Bona Fide Gene Involved in Hominoid Placental Physiology von Mallet, François, Bouton, Olivier, Prudhomme, Sarah, Cheynet, Valérie, Oriol, Guy, Bonnaud, Bertrand, Lucotte, Gérard, Duret, Laurent, Mandrand, Bernard, Coffin, John M.

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Brief communication: Y-chromosome haplotypes in Egypt von Lucotte, G., Mercier, G.

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Celtic Origin of the C282Y Mutation of Hemochromatosis von Lucotte, Gérard

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Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder‐Haplotype Analysis von Yuasa, I., Umetsu, K., Harihara, S., Kido, A., Miyoshi, A., Saitou, N., Dashnyam, B., Jin, F., Lucotte, G., Chattopadhyay, P. K., Henke, L., Henke, J.

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Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia von Ducros, A., Denier, C., Joutel, A., Vahedi, K., Michel, A., Darcel, F., Madigand, M., Guerouaou, D., Tison, F., Julien, J., Hirsch, E., Chedru, F., Bisgård, C., Lucotte, G., Després, P., Billard, C., Barthez, M.A., Ponsot, G., Bousser, M.G., Tournier-Lasserve, E.

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Distribution of Two Asian-Related Coding SNPs in the MC1R and OCA2 Genes von Yuasa, I, Umetsu, K, Harihara, S, Kido, A, Miyoshi, A, Saitou, N, Dashnyam, B, Jin, F, Lucotte, G, Chattopadhyay, P. K, Henke, L, Henke, J

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Frequencies of the CC chemokine receptor 5 Δ32 allele in various populations of defined racial background von Lucotte, G

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Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent von Telenius, H., Kremer, H.P.H., Thellmann, J., Andrew, S.E., Almqvist, E., Anvret, M., Greenberg, C., Greenberg, J., Lucotte, G., Squltierl, F., Starr, A., Goldberg, Y.P., Hayden, M.R.

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Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease von Santt, O., Baranova, H., Albuisson, E., Bignon, Y.-J., Lucotte, G.

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Duplex PCR-RFLP for simultaneous detection of factor V Leiden and prothrombin G20210A von Lucotte, G, Champenois, T

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Molecular basis of the TaqI p49a,f polymorphism in the DYS1 locus containing DAZ genes von Jovelin, F., Berthaud, S., Lucotte, G.

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PCR test for diagnosis of the common GJB2 (connexin 26) 35delG mutation on dried blood spots and determination of the carrier frequency in France von Lucotte, G., Bathelier, C., Champenois, T.

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Y-chromosome DNA haplotypes in Basques von Lucotte, G, Hazout, S

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A de novo heterozygous deletion of 42 base-pairs in the noggin gene of a fibrodysplasia ossificans progressiva patient von Lucotte, G, Sémonin, O, Lutz, P

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Frequencies of 32 base pair deletion of the ( Δ32) allele of the CCR5 HIV-1 co-receptor gene in Caucasians: a comparative analysis von Lucotte, Gérard

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Distribution of the CCR5 gene 32-basepair deletion in West Europe. A hypothesis about the possible dispersion of the mutation by the Vikings in historical times von Lucotte, G

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North African Genes in Iberia Studied by Y-Chromosome DNA Haplotype 5 von LUCOTTE, GÉRARD, GÉRARD, NATHALIE, MERCIER, GÉRALDINE

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Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease : no association found von MERCIER, G, TURPIN, J. C, LUCOTTE, G

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Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay von Lucotte, G, Sesboüé, R

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A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation? von Lucotte, Gérard, Dieterlen, Florent

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