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Publications by authors named "Patricia Talarmain"
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A new mutation of ANO6 in two familial cases of Scott syndrome.
Pierre Boisseau
Marie C Bene
Thomas Besnard
Sinthuja Pachchek
Mathilde Giraud
Patricia Talarmain
Br J Haematol
March 2018
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Molecular misdiagnosis in type 2B von Willebrand disease.
Sebastien Schmitt
Marc Trossaert
Fabrice Airaud
Gaelle Landeau-Trottier
Patricia Talarmain
Am J Hematol
October 2006
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