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Nature Genetics|August 4, 1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, A Colley, R Jamieson, et al.Journal of Medical Genetics|May 19, 2009
Phenotypic expansion and further characterisation of the 17q21.31 microdeletion syndromeT Y Tan, S Aftimos, L Worgan, et al.Nature Genetics|May 20, 1998
Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodiesM Botto, C Dell'Agnola, A E Bygrave, et al.Heredity|July 8, 2010
Local adaptation for body color in Drosophila americanaP J Wittkopp, G Smith-Winberry, L L Arnold, et al.American Journal of Medical Genetics|May 8, 2000
Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotypeL A Brueton, S M Huson, P M Cox, et al.European Cells & Materials|February 16, 2017
Growth plate extracellular matrix-derived scaffolds for large bone defect healingG M Cunniffe, P J Díaz-Payno, J S Ramey, et al.American Journal of Medical Genetics. Part A|September 2, 2003
PEHO and PEHO-like syndromes: report of five Australian casesM J Field, P Grattan-Smith, S M Piper, et al.American Journal of Human Genetics|May 12, 2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, G E Tiller, M Le Merrer, et al.Clinical Genetics|February 18, 2014
Novel KDM6A (UTX) mutations and a clinical and molecular review of the X-linked Kabuki syndrome (KS2)S Banka, D Lederer, V Benoit, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 22, 1998
Multiple lupus susceptibility loci map to chromosome 1 in BXSB miceM B Hogarth, J H Slingsby, P J Allen, et al.Pageof 13