Authors: Tzountzouris, J Kennedy, D Skuterud, M Connolly-Wilson, M Holden, JJA Lin, CC Mak-Tam, E Somerville, MJ Summers, AM Allingham-Hawkins, DJ

Citation: J. Tzountzouris et al., Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome, GENET TEST, 4(3), 2000, pp. 235-239

Authors: Potocki, L Chen, KS Park, SS Osterholm, DE Withers, MA Kimonis, V Summers, AM Meschino, WS Anyane-Yeboa, K Kashork, CD Shaffer, LG Lupski, JR

Citation: L. Potocki et al., Molecular mechanism for duplication 17p11.2 - the homologous recombinationreciprocal of the Smith-Magenis microdeletion, NAT GENET, 24(1), 2000, pp. 84-87

Authors: Summers, AM Summers, CW Drucker, DB Barson, A Hajeer, AH Hutchinson, IV

Citation: Am. Summers et al., Association of IL-10 genotype with sudden infant death syndrome, HUMAN IMMUN, 61(12), 2000, pp. 1270-1273

Authors: Farrell, SA Summers, AM Dallaire, L Singer, J Johnson, JAM Wilson, RD

Citation: Sa. Farrell et al., Club foot, an adverse outcome of early amniocentesis: disruption or deformation?, J MED GENET, 36(11), 1999, pp. 843-846