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Author/Creator Cooper, David N.

4. Analysis of Crossover Breakpoints Yields New Insights into the Nature of the Gene Conversion Events Associated with Large NF1 Deletions Mediated by Nonallelic Homologous Recombination. Issue 2 (2nd December 2013)

Authors:
Bengesser, Kathrin; Vogt, Julia; Mussotter, Tanja; Mautner, Victor‐Felix; Messiaen, Ludwine; Cooper, David N.; Kehrer‐Sawatzki, Hildegard
Journal:
Human mutation
Issue:
Volume 35:Issue 2(2014:Feb.)
Page Start:
215
Record Type:
Journal Article
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6. Clinical heterogeneity of mitochondrial NAD kinase deficiency caused by a NADK2 start loss variant. Issue 3 (1st February 2018)

Authors:
Pomerantz, Daniel J.; Ferdinandusse, Sacha; Cogan, Joy; Cooper, David N.; Reimschisel, Tyler; Robertson, Amy; Bican, Anna; McGregor, Tracy; Gauthier, Jackie; Millington, David S.; Andrae, Jaime L. W.; Tschannen, Michael R.; Helbling, Daniel C.; Demos, Wendy M.; Denis, Simone; Wanders, Ronald J. A...
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 3(2018)
Page Start:
692
Record Type:
Journal Article
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9. Concurrent Nucleotide Substitution Mutations in the Human Genome Are Characterized by a Significantly Decreased Transition/Transversion Ratio. Issue 3 (13th March 2015)

Authors:
Zhu, Wenjuan; Cooper, David N.; Zhao, Qiang; Wang, Ye; Liu, Ruihong; Li, Qibin; Férec, Claude; Wang, Yiming; Chen, Jian‐Min
Journal:
Human mutation
Issue:
Volume 36:Issue 3(2015:Mar.)
Page Start:
333
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗