J. Z. Gu, X. Lin and D.E. Wells. (1996) B22 ubunit of ubiquinone oxidoreductase is a candidate gene for branchio-oto-renal syndrome: Implications for other hearing loss syndromes. Genomics 35: 6-10.
J.Z. Gu, M.J. Wagner, E.A. Haan and D.E. Wells. Detection of a meagbase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS); Implications for mapping and cloning the BOR gene. (1996) Genomics 31:201-209.
M. Sapru, J.Gu, X. Gu, D. Smith, C-E.Yu, D.E. Wells and M.J. Wagner. (1994) A panel of radiation hybrids for human chromosome 8. Genomics 21: 208-216.
J. Gu, L.A. Sadler, S.P. Daiger, D.E. Wells and M.J. Wagner. (1993). Dinucleotide repeat polymorphism at the CRH gene. Human Mol. Genet. 2: 85. abstract
M.J. Wagner, M. Sapru, J. Gu, D.E. Wells. (1992) A panel of radiation hybrids for mapping chromosome 8. American Journal of Human Genetics 51:1591. abstract
D.E. Wells, J. Parrish, J. Hou, M. Sapru, Y. Wang, J. Gu,, A. Cook, S. Blanton, W. Raskind, H. Ludecke, B. Horstemke, and M. J. Wagner. (1993) YAC and cosmid contig maps of chromosome 8. Cytogenetics and Cell Genetics 64:145.abstract
M.J. Wagner, M. Sapru, J.Z. Gu, X Gu, and D.E. Wells. (1993) A radiation hybrid panel for human chromosome 8. American Journal of Human Genetics 53:1368.abstract
J.Z. Gu, E. Brundage, S.P. Daiger, L. Sadler, D.E. Wells and M.J. Wagner. (1993) Combined STS and YAC contig map of proximal 8q, a region containing the RP1 and BOR genes. American Journal of Human Genetics 53:1778.abstract
J.Z. Gu, M. Sapru, D. Smith, J. Hou,, R. Smith, M. Wagner, and D.E. Wells. (1994) Using in situ hybridization to detect translocation breakpoints in a TRPSI/BOR patient cell line. American Journal of Human Genetics 55: A371.abstract
M. Wagner, W. Chen, J. Gu, J. Hou, H. Li, H-J Ludecke and D. E. Wells. (1995) Integrated physical maps of chromosome 8. Cytogenetics and Cell Genetics 68:162.abstract
J.Z. Gu, M.J. Wagner, and D.E. Wells. (1995) Detection of a meagbase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS) and cloning of a candidate BOR gene. American Journal of Human Genetics 57:A1231.