Maloney, Viv K.
Wessex Regional Genetics Laboratory · Salisbury NHS Foundation Trust
2 papers on CoChat
Most cited papers
- Verified
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
Mefford, H. C., Sharp, A. J., Baker, C., Itsara, A., Jiang, Z., Buysse, K., Huang, S., Maloney, V. K., Crolla, J. A., Baralle, D., et al. (2008) · New England Journal of Medicine
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 804
- Verified
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2
Barber, J. C. K., Hall, V., Maloney, V. K., Huang, S., Roberts, A. M., Brady, A. F., Foulds, N., Bewes, B., Volleth, M., Liehr, T., et al. (2013) · European Journal of Human Genetics
Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms
Cited by 74
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