Telomeres and chromosomal instability in chronic lymphocytic leukemia von Véronèse, L, Tournilhac, O, Callanan, M, Prie, N, Kwiatkowski, F, Combes, P, Chauvet, M, Davi, F, Gouas, L, Verrelle, P, Guièze, R, Vago, P, Bay, J O, Tchirkov, A

Volltext

Prenatal BoBs™ in the cytogenetic analysis of products of spontaneous miscarriage von Mellali, S, Haoud, K, Gouas, L, Khaled, M.B, Vago, P, Moulessehoul, S

Volltext

Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjects von GOUAS, L, NICAUD, V, CHAOUCH, S, BERTHET, M, FORHAN, A, TICHET, J, TIRET, L, BALKAU, B, GUICHENEY, P

Volltext

Pronostic de la leucémie lymphoïde chronique : mise au point sur les facteurs biologiques récents von VERONESE, L, TCHIRKOV, A, GOUAS, L, PERISSEL, B, GOUMY, C, VAGO, P

Volltext

Prevalence of aneuploidies in products of spontaneous abortion: Interest of FISH and MLPA von Haoud, K., Mellali, S., Gouas, L., Tchirkov, A., Vago, P., Moulessehoul, S.

Volltext

Prenatal diagnosis of a rare de novo centromeric chromosome 6 variant von Goumy, C., Kemeny, S., Eymard-Pierre, E., Richard, C., Gouas, L., Combes, P., Gay-Bellile, M., Gallot, D., Tchirkov, A., Vago, P.

Volltext

Familial deletion 11q14.3–q22.1 without apparent phenotypic consequences: A haplosufficient 8.5 Mb region von Goumy, C., Gouas, L., Tchirkov, A., Roucaute, T., Giollant, M., Veronèse, L., Francannet, C., Vago, P.

Volltext

A thrombocytosis occurring in Philadelphia positive CML in molecular response to imatinib can reveal an underlying JAK2(V617F) myeloproliferative neoplasm von Véronèse, L, Tchirkov, A, Richard-Pebrel, C, Ledoux-Pilon, A, Fleury, J, Chaleteix, C, Goumy, C, Gouas, L, Berger, M G, Vago, P, Bay, J O, Tournilhac, O

Volltext

Prenatal ultrasound diagnosis of a 48,XXYY syndrome von Kemeny, S., Pebrel-Richard, C., Gouas, L., Veronese, L., Lemery, D., Tchirkov, A., Goumy, C., Vago, P.

Volltext

Gene dosage methods as diagnostic tools for the identification of chromosome abnormalities von Gouas, L., Goumy, C., Véronèse, L., Tchirkov, A., Vago, P.

Volltext

Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p von Goumy, C., Beaufrère, A. M., Tchirkov, A., Gouas, L., Gaspard, F., Giollant, M., Roucaute, T., Veronèse, L., Lemery, D., Vago, P.

Volltext

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population von GOUAS, Laetitia, NICAUD, Viviane, BERTHET, Myriam, FORHAN, Anne, TIRET, Laurence, BALKAU, Beverley, GUICHENEY, Pascale

Volltext

Expression du gène MEST dans les villosités choriales de fœtus trisomiques 21 von Ayed, W., Kémény, S., Goumy, C., Vago, P., Gouas, L.

Volltext

Prognosis of chronic lymphocytic leukemia: focus on recent biomarkers von Véronèse, L, Tchirkov, A, Gouas, L, Périssel, B, Goumy, C, Vago, P

Volltext

De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features von Debost-Legrand, A., Capri, Y., Gouas, L., Pebrel-Richard, C., Veronese, L., Tchirkov, A., Haoud, K., Boespflug-Tanguy, O., Goumy, C., Vago, P.

Volltext

P1232 Unexpected identification of two new KCNQ1 mutations in the general population von GOUAS, L

Volltext

New KCNQ1 mutations leading to haploinsufficiency in a general population1Defective trafficking of a KvLQT1 mutant von GOUAS, L, BELLOCQ, C, BERTHET, M, POTET, F, DEMOLOMBE, S, FORHAN, A, LESCASSE, R, SIMON, F, BALKAU, B, DENJOY, I

Volltext

Trisomie 21 et cancers von Ayed, W., Gouas, L., Penault-Llorca, F., Amouri, A., Tchirkov, A., Vago, P.

Volltext

Prenatal BoBsTM in the cytogenetic analysis of products of spontaneous miscarriage : research von Vago, P., Khaled, M.B., Gouas, L., Haoud, K., Mellali, S., Moulessehoul, S., Haoud, K., Mellali, S.

Volltext

Prenatal BoBs von Mellali, S., Haoud, K., Moulessehoul, S., Gouas, L., Khaled, M.B., Vago, P.

Volltext