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Sandra Hing

Showing results (1-10 of 7) with videos related to

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The Lancet. Oncology|June 1, 2005
Clinical features of molecular pathology of solid tumours in childhoodBoo Messahel, Sandra Hing, Ruth Nash, et al.
Lancet (London, England)|September 21, 2002
Chromosome 1q expression profiling and relapse in Wilms' tumourYong-Jie Lu, Sandra Hing, Richard Williams, et al.
British Journal of Haematology|June 26, 2003
Expression profile of wild-type ETV6 in childhood acute leukaemiaNaina Patel, Lindsey K Goff, Taane Clark, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 17, 2009
GNAS1 mutations occur more commonly than previously thought in intramuscular myxomaDavid Delaney, Tim C Diss, Nadege Presneau, et al.
The Journal of Investigative Dermatology|February 9, 2013
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRASVeronica A Kinsler, Anna C Thomas, Miho Ishida, et al.
Journal of Clinical Pathology|November 29, 2014
Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trialJoshua R Kapp, Tim Diss, James Spicer, et al.
Nature Medicine|January 10, 2024
Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer ProgrammeAlona Sosinsky, John Ambrose, William Cross, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The Lancet. Oncology|June 1, 2005
Clinical features of molecular pathology of solid tumours in childhoodBoo Messahel, Sandra Hing, Ruth Nash, et al.
Lancet (London, England)|September 21, 2002
Chromosome 1q expression profiling and relapse in Wilms' tumourYong-Jie Lu, Sandra Hing, Richard Williams, et al.
British Journal of Haematology|June 26, 2003
Expression profile of wild-type ETV6 in childhood acute leukaemiaNaina Patel, Lindsey K Goff, Taane Clark, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 17, 2009
GNAS1 mutations occur more commonly than previously thought in intramuscular myxomaDavid Delaney, Tim C Diss, Nadege Presneau, et al.
The Journal of Investigative Dermatology|February 9, 2013
Multiple congenital melanocytic nevi and neurocutaneous melanosis are caused by postzygotic mutations in codon 61 of NRASVeronica A Kinsler, Anna C Thomas, Miho Ishida, et al.
Journal of Clinical Pathology|November 29, 2014
Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trialJoshua R Kapp, Tim Diss, James Spicer, et al.
Nature Medicine|January 10, 2024
Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer ProgrammeAlona Sosinsky, John Ambrose, William Cross, et al.
Pageof 1