Hélène Cavé - Dissemin

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Papers authored by Hélène Cavé

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2006 Tetsuya Niihori, Yoko Aoki, Yoko Narumi, Giovanni Neri, Hélène Cavé, Alain Verloes, Nobuhiko Okamoto, Raoul C. M. Hennekam, Gabriele Gillessen-Kaesbach, Dagmar Wieczorek, Maria Ines Kavamura, Kenji Kurosawa, Hirofumi Ohashi, Louise Wilson, Delphine Héron and 9 other authors

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

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Jean-Marc Levaillant, Marion Gérard-Blanluet, Muriel Holder-Espinasse, Anne-Sylvie Valat-Rigot, Louise Devisme, Hélène Cavé, Sylvie Manouvrier-Hanu

Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri-dimensional ultrasonography

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2005 Nelly Robillard, Hélène Cavé, Françoise Méchinaud, Christine Guidal, Francine Garnache-Ottou, Pierre-Simon Rohrlich, Hervé Avet-Loiseau

ORCID

, Richard Garand

Four-color flow cytometry bypasses limitations of IG/TCR polymerase chain reaction for minimal residual disease detection in certain subsets of children with acute lymphoblastic leukemia.

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Lisa Giovannini, Hélène Cavé, Corinne Ferrero-Vacher, Patrick Boutte, Nicolas Sirvent

A new PTPN11 mutation in juvenile myelomonocytic leukaemia associated with Noonan syndrome

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2004 Martine Vaxillaire, Céline Populaire, Kanetee Busiah, Hélène Cavé, Anna L. Gloyn, Andrew T. Hattersley, Paul Czernichow, Philippe Froguel, Michel Polak

Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.

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2002 Chantal Metz, Hélène Cavé, Anne Marie Bertrand, Christine Deffert, Béatrice Gueguen-Giroux, Paul Czernichow, Michel Polak

Neonatal diabetes mellitus: Chromosomal analysis in transient and permanent cases

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1997 Patricia Mariani-Kurkdjian, Hélène Cavé, Jacques Elion, Chantal Loirat, Edouard Bingen

Direct detection of verotoxin genes in stool samples by polymerase chain reaction in hemolytic uremic syndrome patients in France

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1995 Emmanuel Martin, Valère Cacheux, Hélène Cavé, Jean Michel Lapierre, Denis Le Paslier, Bernard Grandchamp

Localization of the CDKN4/p27Kip1 gene to human chromosome 12p12.3

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