SMARCB1/INI1 Involvement in Pediatric Chordoma: A Mutational and Immunohistochemical Analysis.
about
Genetic aberrations and molecular biology of skull base chordoma and chondrosarcoma.Chordoma Occurs in Young Children With Tuberous Sclerosis.Oncogenic roles of SMARCB1/INI1 and its deficient tumorsSNF5 as a prognostic factor in skull base chordoma.Poorly differentiated chordoma with loss of SMARCB1/INI1 expression in pediatric patients: A report of two cases and review of the literature.
P2860
SMARCB1/INI1 Involvement in Pediatric Chordoma: A Mutational and Immunohistochemical Analysis.
description
2016 nî lūn-bûn
@nan
2016 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@ast
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@en
type
label
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@ast
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@en
prefLabel
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@ast
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@en
P2093
P50
P1476
SMARCB1/INI1 Involvement in Pe ...... Immunohistochemical Analysis.
@en
P2093
Alessandro Raso
Antonella Coli
Antonietta Arcella
Francesca R Buttarelli
Manila Antonelli
Marco Gessi
Marina P Gardiman
Samantha Mascelli
P356
10.1097/PAS.0000000000000741
P407
P577
2016-09-15T00:00:00Z