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All papers authored by Mathias Schwartz

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2019 Mathias Schwartz

ORCID

, Clement Korenbaum, Meriem Benfoda, Mickael Mary, Chrystelle Colas, Florence Coulet, Melissa Parrin, Philippe Jonveaux, Olivier Ingster, Sandra Granier, Louis De Mestier, Jerome Cros, Angelique Riffault, Marie Muller, Philippe Levy and 4 other authors

Familial pancreatic adenocarcinoma: A retrospective analysis of germline genetic testing in a French multicentre cohort

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This paper was not found in any repository, but could be made available legally by the author.

2018 Stéphanie Baert-Desurmont, Sophie Coutant, Françoise Charbonnier, Pierre Macquere, François Lecoquierre

ORCID

, Mathias Schwartz

ORCID

, Maud Blanluet, Myriam Vezain, Raphaël Lanos, Olivier Quenez, Jacqueline Bou, Emilie Bouvignies, Steeve Fourneaux, Sandrine Manase, Stéphanie Vasseur and 7 other authors

Optimization of the diagnosis of inherited colorectal cancer using NGS and capture of exonic and intronic sequences of panel genes

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This paper was not found in any repository, but could be made available legally by the author.

2017 Mathias Schwartz

ORCID

, Damien Sternberg, Sandra Whalen, Alexandra Afenjar, Arnaud Isapof, Brigitte Chabrol, Marie-France Portnoï, Solveig Heide, Boris Keren, Sandra Chantot-Bastaraud, Jean-Pierre Siffroi

How chromosomal deletions can unmask recessive mutations? Deletions in 10q11.2 associated with CHAT or SLC18A3 mutations lead to congenital myasthenic syndrome

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