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Parallel molecular genetic analysis.
McKenzie SE, Mansfield E, Rappaport E, Surrey S, Fortina P. McKenzie SE, et al. Among authors: mansfield e. Eur J Hum Genet. 1998 Sep-Oct;6(5):417-29. doi: 10.1038/sj.ejhg.5200218. Eur J Hum Genet. 1998. PMID: 9801865 Review.
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.
Zelante L, Gasparini P, Estivill X, Melchionda S, D'Agruma L, Govea N, Milá M, Monica MD, Lutfi J, Shohat M, Mansfield E, Delgrosso K, Rappaport E, Surrey S, Fortina P. Zelante L, et al. Among authors: mansfield e. Hum Mol Genet. 1997 Sep;6(9):1605-9. doi: 10.1093/hmg/6.9.1605. Hum Mol Genet. 1997. PMID: 9285800
Nucleic acid detection using non-radioactive labelling methods.
Mansfield ES, Worley JM, McKenzie SE, Surrey S, Rappaport E, Fortina P. Mansfield ES, et al. Mol Cell Probes. 1995 Jun;9(3):145-56. doi: 10.1006/mcpr.1995.0023. Mol Cell Probes. 1995. PMID: 7477006 Free article. Review.
249 results