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Samuel Clokie

Showing results (1-10 of 14) with videos related to

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The FEBS Journal|October 29, 2009
The interaction between casein kinase Ialpha and 14-3-3 is phosphorylation dependentSamuel Clokie, Helen Falconer, Shaun Mackie, et al.
Prenatal Diagnosis|January 30, 2016
Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosageMichael Parks, Samantha Court, Siobhan Cleary, et al.
European Journal of Human Genetics : EJHG|January 26, 2017
Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosageMichael Parks, Samantha Court, Benjamin Bowns, et al.
Journal of Neurochemistry|July 30, 2011
Crx broadly modulates the pineal transcriptomeLouise Rovsing, Samuel Clokie, Diego M Bustos, et al.
The British Journal of Ophthalmology|February 13, 2019
Non-invasive diagnosis of retinoblastoma using cell-free DNA from aqueous humourAmy Gerrish, Edward Stone, Samuel Clokie, et al.
The Journal of Molecular Diagnostics : JMD|June 20, 2020
Clinical Service Delivery of Noninvasive Prenatal Diagnosis by Relative Haplotype Dosage for Single-Gene DisordersElizabeth Young, Benjamin Bowns, Amy Gerrish, et al.
European Journal of Human Genetics : EJHG|October 7, 2022
Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxiaFabiola Ceroni, Daniel Osborne, Samuel Clokie, et al.
Molecular Diagnosis & Therapy|October 8, 2017
Increased Sensitivity of Diagnostic Mutation Detection by Re-analysis Incorporating Local Reassembly of Sequence ReadsChristopher M Watson, Nick Camm, Laura A Crinnion, et al.
Journal of Clinical Medicine|November 4, 2020
Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritance by Combined Targeted Sequencing StrategiesAmy Gerrish, Benjamin Bowns, Chipo Mashayamombe-Wolfgarten, et al.
American Journal of Human Genetics|September 9, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
The FEBS Journal|October 29, 2009
The interaction between casein kinase Ialpha and 14-3-3 is phosphorylation dependentSamuel Clokie, Helen Falconer, Shaun Mackie, et al.
Prenatal Diagnosis|January 30, 2016
Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosageMichael Parks, Samantha Court, Siobhan Cleary, et al.
European Journal of Human Genetics : EJHG|January 26, 2017
Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosageMichael Parks, Samantha Court, Benjamin Bowns, et al.
Journal of Neurochemistry|July 30, 2011
Crx broadly modulates the pineal transcriptomeLouise Rovsing, Samuel Clokie, Diego M Bustos, et al.
The British Journal of Ophthalmology|February 13, 2019
Non-invasive diagnosis of retinoblastoma using cell-free DNA from aqueous humourAmy Gerrish, Edward Stone, Samuel Clokie, et al.
The Journal of Molecular Diagnostics : JMD|June 20, 2020
Clinical Service Delivery of Noninvasive Prenatal Diagnosis by Relative Haplotype Dosage for Single-Gene DisordersElizabeth Young, Benjamin Bowns, Amy Gerrish, et al.
European Journal of Human Genetics : EJHG|October 7, 2022
Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxiaFabiola Ceroni, Daniel Osborne, Samuel Clokie, et al.
Molecular Diagnosis & Therapy|October 8, 2017
Increased Sensitivity of Diagnostic Mutation Detection by Re-analysis Incorporating Local Reassembly of Sequence ReadsChristopher M Watson, Nick Camm, Laura A Crinnion, et al.
Journal of Clinical Medicine|November 4, 2020
Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritance by Combined Targeted Sequencing StrategiesAmy Gerrish, Benjamin Bowns, Chipo Mashayamombe-Wolfgarten, et al.
American Journal of Human Genetics|September 9, 2017
Dominant Mutations in GRM1 Cause Spinocerebellar Ataxia Type 44Lauren M Watson, Elizabeth Bamber, Ricardo Parolin Schnekenberg, et al.
Pageof 2