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Author/Creator Coates, Andrea

4. Diagnostic whole genome sequencing and split‐read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome. Issue 10 (16th July 2014)

Authors:
Watson, Christopher M.; Crinnion, Laura A.; Tzika, Antigoni; Mills, Alison; Coates, Andrea; Pendlebury, Maria; Hewitt, Sarah; Harrison, Sally M.; Daly, Catherine; Roberts, Paul; Carr, Ian M.; Sheridan, Eamonn G.; Bonthron, David T.
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 10(2014.)
Page Start:
2649
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Diagnostic whole genome sequencing and split‐read mapping for nucleotide resolution breakpoint identification in CNTNAP2 deficiency syndrome. Issue 10 (16th July 2014)

Authors:
Watson, Christopher M.; Crinnion, Laura A.; Tzika, Antigoni; Mills, Alison; Coates, Andrea; Pendlebury, Maria; Hewitt, Sarah; Harrison, Sally M.; Daly, Catherine; Roberts, Paul; Carr, Ian M.; Sheridan, Eamonn G.; Bonthron, David T.
Journal:
American journal of medical genetics
Issue:
Volume 164:Issue 10(2014.)
Page Start:
2649
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗