V. Hall

Methylation-sensitive high-resolution melting-curve analysis of the SNRPN gene as a diagnostic screen for Prader-Willi and Angelman syndromes.

N. Cross, H. White, V. Hall, 2007, Clinical chemistry.

A certi fi ed plasmid reference material for the standardisation of BCR – ABL1 mRNA quanti fi cation by real-time quantitative PCR

D. Colomer, T. Lion, M. Jansson, 2015 .

RUNX1 mutations correlate with response to venetoclax combination therapies in relapsed/refractory acute myeloid leukemia.

Steven M. Chan, Signy Chow, Rosemarie Tremblay-Lemay, 2021, Leukemia research.

Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus

H E White, W. Tapper, J. Dumanski, 2015, Leukemia.

Evaluation of a Novel Assay for Detection of the Fetal Marker RASSF1A: Facilitating Improved Diagnostic Reliability of Noninvasive Prenatal Diagnosis

J. Crolla, H. White, L. Chitty, 2012, PloS one.

16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2

Shuwen Huang, V. Maloney, J. Barber, 2012, European Journal of Human Genetics.

A certified plasmid reference material for the standardisation of BCR–ABL1 mRNA quantification by real-time quantitative PCR

H Emons, V Kairisto, S Trapmann, 2014, Leukemia.