检索结果 - S Grandjouan

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  1. 1
    Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers

    Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers 由 A. Haliassos, Jean‐Claude Chomel, S Grandjouan, J Kruh, J.‐C. Kaplan, Alain Kitzis

    出版 1989
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  2. 2
    Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers.

    Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers. 由 Haliassos, A, Chomel, J C, Grandjouan, S, Kruh, J, Kaplan, J C, Kitzis, A

    出版 1989
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  3. 3
    Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

    Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. 由 Henry, I, Grandjouan, S, Couillin, P, Barichard, F, Huerre-Jeanpierre, C, Glaser, T, Philip, T, Lenoir, G, Chaussain, J L, Junien, C

    出版 1989
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    Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma.

    Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. 由 Isabelle Henry, S Grandjouan, P. Couillin, F. Barichard, Marc Jeanpierre, Thomas Gläser, Thierry Philip, Gilbert Lenoir, J. L. Chaussain, Claudine Junien

    出版 1989
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  5. 5
    Extensive molecular screening for hereditary non-polyposis colorectal cancer

    Extensive molecular screening for hereditary non-polyposis colorectal cancer 由 Dieumegard, B, Grandjouan, S, Sabourin, J-C, Bihan, M-L Le, Lefrère, I, Bellefqih, Pignon, J-P, Rougier, P, Lasser, P, Bénard, J, Couturier, D, Bressac-de Paillerets, B

    出版 2000
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    Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents

    Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents 由 Sahra Bodo, Chrystelle Colas, Olivier Buhard, Ada Collura, Julie Tinat, Noémie Lavoine, Agathe Guilloux, Alexandra Chalastanis, Philippe Lafitte, Florence Coulet, Marie‐Pierre Buisine, Denisa Ilenčíková, Clara Ruíz-Ponte, Miriam Kinzel, S Grandjouan, Hilde Brems, Sophie Lejeune, Hélène Blanché, Qing Wang, Olivier Caron, Odile Cabaret, Magali Svrcek, Dominique Vidaud, Béatrice Parfait, Alain Verloès, Ulrich J. Knappe, Florent Soubrier, Isabelle Mortemousque, Alexander Leis, Jessie Auclair‐Perrossier, Thierry Frébourg, Jean–François Fléjou, Natacha Entz‐Werlé, Julie Leclerc, David Malka, Odile Cohen‐Haguenauer, Yael Goldberg, Anne‐Marie Gerdes, Faten Fedhila, Michèle Mathieu‐Dramard, Richard Hamelin, Wafaa Badre, Marion Gauthier‐Villars, Franck Bourdeaut, Eamonn Sheridan, Hans F. A. Vasen, Laurence Brugières, Katharina Wimmer, Martine Muleris, Alex Duval

    出版 2015
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