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Author/Creator Bowles, Karla

1. A substantial proportion of apparently heterozygous TP53 pathogenic variants detected with a next‐generation sequencing hereditary pan‐cancer panel are acquired somatically. Issue 1 (23rd September 2019)

Authors:
Coffee, Bradford; Cox, Hannah C.; Bernhisel, Ryan; Manley, Susan; Bowles, Karla; Roa, Benjamin B.; Mancini‐DiNardo, Debora
Journal:
Human mutation
Issue:
Volume 41:Issue 1(2020)
Page Start:
203
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel. Issue 1 (3rd September 2014)

Authors:
Tung, Nadine; Battelli, Chiara; Allen, Brian; Kaldate, Rajesh; Bhatnagar, Satish; Bowles, Karla; Timms, Kirsten; Garber, Judy E.; Herold, Christina; Ellisen, Leif; Krejdovsky, Jill; DeLeonardis, Kim; Sedgwick, Kristin; Soltis, Kathleen; Roa, Benjamin; Wenstrup, Richard J.; Hartman, Anne‐Renee
Journal:
Cancer
Issue:
Volume 121:Issue 1(2015)
Page Start:
25
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next‐generation sequencing with a 25‐gene panel. Issue 1 (3rd September 2014)

Authors:
Tung, Nadine; Battelli, Chiara; Allen, Brian; Kaldate, Rajesh; Bhatnagar, Satish; Bowles, Karla; Timms, Kirsten; Garber, Judy E.; Herold, Christina; Ellisen, Leif; Krejdovsky, Jill; DeLeonardis, Kim; Sedgwick, Kristin; Soltis, Kathleen; Roa, Benjamin; Wenstrup, Richard J.; Hartman, Anne‐Renee
Journal:
Cancer
Issue:
Volume 121:Issue 1(2015)
Page Start:
25
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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