Child Neurology: RNA Sequencing for the Diagnosis of Lissencephaly
暂无分享,去创建一个
Arun K. Ramani | M. Brudno | A. Ramani | J. Dowling | H. Gonorazky | S. Naumenko | K. Amburgey | H. Qashqari | M. M. Ghahramani Seno | Soma Das
[1] A. Poduri,et al. Genetic diagnoses in epilepsy: The impact of dynamic exome analysis in a pediatric cohort , 2020, Epilepsia.
[2] I. Krantz,et al. Diagnosing Cornelia de Lange syndrome and related neurodevelopmental disorders using RNA sequencing , 2019, Genetics in Medicine.
[3] Michael Brudno,et al. Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease , 2019, American journal of human genetics.
[4] Daniele Merico,et al. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test , 2017, Genetics in Medicine.
[5] Francesco Muntoni,et al. Improving genetic diagnosis in Mendelian disease with transcriptome sequencing , 2016, Science Translational Medicine.
[6] J. Carpten,et al. Translating RNA sequencing into clinical diagnostics: opportunities and challenges , 2016, Nature Reviews Genetics.
[7] Eric Vilain,et al. Clinical exome sequencing for genetic identification of rare Mendelian disorders. , 2014, JAMA.
[8] W. Dobyns,et al. PAFAH1B1-Associated Lissencephaly/Subcortical Band Heterotopia , 2014 .
[9] A. James Barkovich,et al. Malformations of cortical development and epilepsy , 2001, Brain and Development.