Authors: Stalker, HJ Gray, BA Zori, RT

Citation: Hj. Stalker et al., Dominant transmission of a previously unidentified 13/17 translocation in a five-generation family with Robin cleft and other skeletal defects, AM J MED G, 103(4), 2001, pp. 339-341

Authors: Gray, BA Bent-Williams, A Wolff, DJ Zori, RT

Citation: Ba. Gray et al., A non-sex chromosome marker in a patient with an atypical Ullrich-Turner phenotype and mosaicism of 46,X,mar/46,XX, CLIN GENET, 60(1), 2001, pp. 73-76

Authors: Wallace, MR Rasmussen, SA Lim, IT Gray, BA Zori, RT Muir, D

Citation: Mr. Wallace et al., Culture of cytogenetically abnormal Schwann cells from benign and malignant NFI tumors, GENE CHROM, 27(2), 2000, pp. 117-123

Authors: Marsh, DJ Kum, JB Lunetta, KL Bennett, MJ Gorlin, RJ Ahmed, SF Bodurtha, J Crowe, C Curtis, MA Dasouki, M Dunn, T Feit, H Geraghty, MT Graham, JM Hodgson, SV Hunter, A Korf, BR Manchester, D Miesfeldt, S Murday, VA Nathanson, KL Parisi, M Pober, B Romano, C Tolmie, JL Trembath, R Winter, RM Zackai, EH Zori, RT Weng, LP Dahia, PLM Eng, C

Citation: Dj. Marsh et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome, HUM MOL GEN, 8(8), 1999, pp. 1461-1472

Authors: Boyadjiev, SA Jabs, EW LaBuda, M Jamal, JE Torbergsen, T Ptacek, LJ Rogers, RC Nyberg-Hansen, R Opjordsmoen, S Zeller, CB Stine, OC Stalker, HJ Zori, RT Shapiro, RE

Citation: Sa. Boyadjiev et al., Linkage analysis narrows the critical region for oculodentodigital dysplasia to chromosome 6q22-q23, GENOMICS, 58(1), 1999, pp. 34-40

Authors: Zori, RT Marsh, DJ Graham, GE Marliss, EB Eng, C

Citation: Rt. Zori et al., Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome, AM J MED G, 80(4), 1998, pp. 399-402