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.
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.
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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