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	Title	Author(s)	Issue Date	Views
	Molecular and mutation analysis of hereditary multiple exostoses Proceeding/Conference:British Cancer Research Meeting	Hui, WS Cheah, KSE Huang, J Cheung, KMC Yang, L Luo, ZJ Savarirayan, R Chan, D	2002	115
	Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia Journal:American Journal of Human Genetics	CamposXavier, AB Martinet, D Bateman, J Belluoccio, D Rowley, L Tan, TY Baxová, A Gustavson, KH Borochowitz, ZU Innes, AM Unger, S Beckmann, JS Mittaz, L Ballhausen, D SupertiFurga, A Savarirayan, R Bonafé, L	2009	60
	Novel quantitative trait loci for central corneal thickness identiWed by candidate gene analysis of osteogenesis imperfecta genes Journal:Human Genetics	Dimasi, DP Chen, JY Hewitt, AW Klebe, S Richard, D Stirling, J Thompson, E Forbes, R Tan, TY Savarirayan, R Mackey, DA Healey, PR Mitchell, P Burdon, KP Craig, JE	2010	42
	A patient with monosomy 1p36, atypical features and phenotypic similarities with Cantu syndrome Journal:American Journal of Medical Genetics	Tan, TY Bankier, A Slater, HR Northrop, EL Zacharin, M Savarirayan, R	2005	52
	A patient with Mullerian abnormalities, renal dysplasia, cervical spine fusion, cataracts and intellectual disability: MURCS-plus? Journal:Clinical Dysmorphology	Tan, TY Whitelaw, C Savarirayan, R	2007	40
	Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndrome Journal:Journal of Medical Genetics	Tan, TY Aftimos, S Worgan, L Susman, R Wilson, M Ghedia, S Kirk, EP Love, D Ronan, A Darmanian, A Slavotinek, A Hogue, J Moeschler, JB Ozmore, J Widmer, R Savarirayan, R Peters, G	2009	70
	Two sisters with IMAGe syndrome: Cytomegalic adrenal histopathology, support for autosomal recessive inheritance and literature review Journal:American Journal of Medical Genetics, Part A	Tan, TY Jameson, JL Campbell, PE Ekert, PG Zacharin, M Savarirayan, R	2006	49

Showing results 3 to 9 of 9 < previous