Browsing by Author Wilson, Meredith J.

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Issue DateTitleAuthor(s)Citation
2010The natural history and osteodystrophy of mucolipidosis types II and IIIMunns, Craig; Sillence, David; Alcausin, Melanie; Ault, Jenny E.; Briody, Julie N.; Cathey, Sara; David-Vizcarra, Grace; Edwards, Matthew J.; Fietz, M.; Fletcher, Janice; McGill, Jim; Savarirayan, Ravi; Wilson, Meredith J.; Children's Hospital Westmead: Paediatrics & Child Health; Children's Hospital Westmead: Paediatrics & Child HealthThe natural history and osteodystrophy of mucolipidosis types II and III, Journal of Paediatrics and Child Health, vol.46, 6, 2010,pp 316-322
2009Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndromePeters, Gregory; Widmer, Richard; Aftimos, Salim; Darmanian, Artur; et al, various; Ghedia, S; Kirk, E. P. E.; Love, Donald; Ronan, A; Susman, Rachel D.; Tan, T; Wilson, Meredith J.; Worgan, L; Children's Hospital Westmead: Paediatrics & Child Health; Dentistry FacultyPhenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome, Journal of Medical Genetics, vol.46, 7,pp 480-489
2013A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same familyGrigg, John; Jamieson, Robyn; Ng, W; Bardakjian, T; Mackey, G; Pasutto, Francesca; Schneider, A; Watson, G; Wilson, Meredith J.; Zenker, M; Central Clinical School: Clinical Ophthal & Eye Health; Children's Hospital Westmead: Paediatrics & Child Health; Central Clinical School: Save Sight & Eye Health Inst.A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family, Clinical Genetics, vol.83, 2, 2013,pp 162-168