Targeted sequencing using a 47 gene multiple myeloma mutation panel (M3P) in ‐17p high risk disease

Publisher： John Wiley & Sons Inc

E-ISSN： 1365-2141|168|4|507-510

ISSN： 0007-1048

Source： BRITISH JOURNAL OF HAEMATOLOGY, Vol.168, Iss.4, 2015-02, pp. : 507-510

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2‐p12) deletion

By  

MUSCLE AND NERVE, Vol. 148-639X, Iss. 5, 2015-11 ,pp. : 905-908

John Wiley & Sons Inc

Access to resources Recommend Favorite

Coexistence of a T118M PMP22 missense mutation and chromosome 17 (17p11.2‐p12) deletion

By  

MUSCLE AND NERVE, Vol. 52, Iss. 5, 2015-11 ,pp. : 905-908

John Wiley & Sons Inc

Access to resources Recommend Favorite

Next‐generation sequencing targeted disease panel in rod‐cone retinal dystrophies in Māori and Polynesian reveals novel changes and a common founder mutation

By  

CLINICAL & EXPERIMENTAL OPHTHALMOLOGY, Vol. 45, Iss. 9, 2017-12 ,pp. : 901-910

John Wiley & Sons Inc

Access to resources Recommend Favorite

Comment on ‘p.E66Q mutation in the GLA gene is associated with a high risk of cerebral small‐vessel occlusion in elderly Japanese males’

By  

EUROPEAN JOURNAL OF NEUROLOGY, Vol. 21, Iss. 8, 2014-08 ,pp. : e62-e62

John Wiley & Sons Inc

Access to resources Recommend Favorite

Racial/ethnic disparities in inflammatory gene single‐nucleotide polymorphisms as predictors of a high risk for symptom burden in patients with multiple myeloma 1 year after diagnosis

By  

CANCER, Vol. 121, Iss. 7, 2015-04 ,pp. : 1138-1146

John Wiley & Sons Inc

Access to resources Recommend Favorite