Association of paediatric mastocytosis with a polymorphism resulting in an amino acid substitution (M541L) in the transmembrane domain of c-KIT
Foster, R., Byrnes, E., Ashman, L. K., Meldrum, C., Griffith, R., Ross, G., Upjohn, E., Braue, A., Scott, R., Varigos, G., Ferrao, P.
A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology
Talseth-Palmer, B. A., Bowden, N. A., Scott, R. J., Meldrum, C., Nicholl, J., Thompson, E., Friend, K., Liebelt, J., Bratkovic, D., Haan, E., Yu, S.
cDNA analysis of the BRCA1 unclassified variant c.5194-12G > A (letter)
Wong-Brown, M. W., McPhillips, M. L., Hipwell, M., Pecenpetelovska, G., Dooley, S., Meldrum, C., Scott, R. J.
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