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Revolutionising genetic testin...
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Revolutionising genetic testing for Ataxias using Next Generation Sequencing (NGS)
Manylion Llyfryddiaeth
Prif Awduron:
Nemeth, A
,
Kwasniewska, A
,
Schnekenberg, R
,
Lise, S
,
Becker, E
,
Shanks, M
,
Cader, M
,
Talbot, K
,
de Silva, R
,
Fletcher, N
,
Hastings, R
,
Jayawant, S
,
Lunt, P
,
Morrisor, P
,
Worth, P
,
Tolmie, J
,
Packham, E
,
Seller, A
,
Ragoussis, J
Fformat:
Conference item
Cyhoeddwyd:
2012
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Disgrifiad
Crynodeb:
Eitemau Tebyg
Next Generation Sequencing (NGS) of Genes Associated with Congenital and Neurodegenerative Ataxia
gan: Kwasniewska, A, et al.
Cyhoeddwyd: (2011)
Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model
gan: Németh, A, et al.
Cyhoeddwyd: (2013)
Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model.
gan: Németh, A, et al.
Cyhoeddwyd: (2013)
Targeted Capture and Next Generation Sequencing (NGS) of genes involved in Inherited Retinal Degeneration (IRD)
gan: Shanks, M, et al.
Cyhoeddwyd: (2011)
Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease.
gan: Shanks, M, et al.
Cyhoeddwyd: (2013)