Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency.
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Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency.
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2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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name
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@ast
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@en
type
label
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@ast
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@en
prefLabel
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@ast
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@en
P2093
P2860
P356
P1476
Whole Exome- and mRNA-Sequenci ...... Context of SMARCB1 Deficiency.
@en
P2093
Ana Maria Marino
Johanna Sandgren
Jurate Asmundsson
Monica Nistér
Pernilla Grillner
Stefan Holm
Teresita Díaz de Ståhl
P2860
P304
P356
10.1155/2015/862039
P407
P577
2015-08-12T00:00:00Z