Associated Papers
Next-generation sequencing based detection of germline and somatic alterations in a patient with four metachronous primary tumors.
Martin M et al.
Gynecologic Oncology Reports, 2018
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.
Marchetti G et al.
British Journal of Haematology, 1995
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