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1. 116 Exome Sequencing Uncovers Molecular Determinants of Trigeminal Neuralgia. Issue Volume 65:Issue CN(2018)Supplement 1 (16th August 2018)

2. 125 De Novo Mutations in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus. Issue Volume 65:Issue CN(2018)Supplement 1 (16th August 2018)

3. 169 Exome Sequencing Implicates Endothelial Ras Signaling Network in Vein of Galen Aneurysmal Malformation. (April 2023)

4. Abstract 24: Two Locus Inheritance of Non-Syndromic Midline Craniosynostosis Via Rare SMAD6 and Common BMP2 Alleles. Issue 4 (April 2017)

7. Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing. (9th January 2015)

8. Distal hereditary motor neuronopathy of the Jerash type is caused by a novel SIGMAR1 c.500A>T missense mutation. Issue 3 (11th September 2019)

9. Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation. (1st September 2019)

10. Exome Sequencing Implicates SWI/SNF Chromatin Remodeling Genes in Human Congenital Hydrocephalus. (1st September 2019)