Authors: Chalmers, FM Curnow, KM

Citation: Fm. Chalmers et Km. Curnow, Scaling up the ligase chain reaction-based approach to gene synthesis, BIOTECHNIQU, 30(2), 2001, pp. 249

Authors: Portrat, S Mulatero, P Curnow, KM Chaussain, JL Morel, Y Pascoe, L

Citation: S. Portrat et al., Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11 beta-hydroxylase) and CYP11B2 (aldosterone synthase) cause steroid 11 beta-hydroxylase deficiency and congenital adrenal hyperplasia, J CLIN END, 86(7), 2001, pp. 3197-3201

Authors: Nikkila, H McMillan, DR Nunez, BS Pascoe, L Curnow, KM White, PC

Citation: H. Nikkila et al., Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain, MOL ENDOCR, 14(9), 2000, pp. 1351-1364

Authors: Curnow, KM Pham, T August, P

Citation: Km. Curnow et al., The L10F mutation of angiotensinogen is rare in pre-eclampsia, J HYPERTENS, 18(2), 2000, pp. 173-178

Authors: Cerame, BI Newfield, RS Pascoe, L Curnow, KM Nimkarn, S Roe, TF New, MI Wilson, RC

Citation: Bi. Cerame et al., Prenatal diagnosis and treatment of 11 beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia, J CLIN END, 84(9), 1999, pp. 3129-3134