Genetic testing and immunohistochemistry for SDHB in phaeochromocytoma-paraganglioma syndromes: the South Australian experience von Poplawski, NK, Rawlings, L, Seymour, J, Vakulin, C, Tirimacco, A, Benn, DE, Gill, AJ

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An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers von Madorsky-Feldman, Dana, Sklair-Levy, Miri, Perri, Tamar, Laitman, Yael, Paluch-Shimon, Shani, Schmutzler, Rita, Rhiem, Kerstin, Lester, Jenny, Karlan, Beth Y., Singer, Christian F., Van Maerken, Tom, Claes, Kathleen, Brunet, Joan, Izquierdo, Angel, Teulé, Alex, Lee, Jong Won, Kim, Sung-Won, Arun, Banu, Jakubowska, Anna, Lubinski, Jan, Tucker, Katherine, Poplawski, Nicola K., Varesco, Liliana, Bonelli, Luigina Ada, Buys, Saundra S., Mitchell, Gillian, Tischkowitz, Marc, Gerdes, Anne-Marie, Seynaeve, Caroline, Robson, Mark, Kwong, Ava, Tung, Nadine, Tessa, Nalven, Domchek, Susan M., Godwin, Andrew K., Rantala, Johanna, Arver, Brita, Friedman, Eitan

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Investigating intellectual disability: A genetic perspective von Poplawski, NK

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Passive exposure to tobacco smoke and bacterial meningitis in children von Iles, K, Poplawski, NK, Couper, RTL

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Treatment of late‐onset nonketotic hyperglycinaemia: Effectiveness of imipramine and benzoate von Wiltshire, E. J., Poplawski, N. K., Harrison, J. R., Fletcher, J. M.

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Urine amino and organic acids analysis in developmental delay or intellectual disability von Poplawski, NK, Harrison, JR, Norton, W, Wiltshire, E, Fletcher, JM

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Analysis of CFTR mutation screening in cases of isolated fetal echogenic bowel in the South Australian population von Nicholls, C. M., Nelson, P. V., Poplawski, N. K., Chin, S. J., Fong, B. A., Solly, P. B., Fietz, M. J., Fletcher, J. M.

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Ornithine carbamoyltransferase deficiency presenting with chorea in a female von Wiltshire, E. J., Poplawski, N. K., Harbord, M. G., Harrison, R. J., Fletcher, J. M.

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