Authors: Mumm, S Zhang, XF Gottesman, GS McAlister, WH Whyte, MP

Citation: S. Mumm et al., Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin, J BONE MIN, 16(12), 2001, pp. 2245-2250

Authors: Batanian, JR Huang, YF Gottesman, GS Grange, DK Blasingame, AV

Citation: Jr. Batanian et al., Preferential involvement of the short arm in chromosome 8-derived supernumerary markers and ring as identified by chromosome arm painting, AM J MED G, 90(4), 2000, pp. 276-282

Authors: Mumm, S Christie, PT Finnegan, P Jones, J Dixon, PH Pannett, AAJ Harding, B Gottesman, GS Thakker, RV Whyte, MP

Citation: S. Mumm et al., A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred, J CLIN END, 85(9), 2000, pp. 3343-3347

Authors: Whyte, MP Gottesman, GS Eddy, MC McAlister, WH

Citation: Mp. Whyte et al., X-linked recessive spondyloepiphyseal dysplasia tarda - Clinical and radiographic evolution in a 6-generation kindred and review of the literature, MEDICINE, 78(1), 1999, pp. 9-25

Authors: Gottesman, GS Hoffmann, JW Vogler, C Chen, SC

Citation: Gs. Gottesman et al., Hypertrophic cardiomyopathy in a newborn infant, J PEDIAT, 134(1), 1999, pp. 114-118