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Results: 1-10 |
Results: 10
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
Authors: Bespalova, IN Van Camp, G Bom, SJH Brown, DJ Cryns, K DeWan, AT Erson, AE Flothmann, K Kunst, HPM Kurnool, P Sivakumaran, TA Cremers, CWRJ Leal, SM Burmeister, M Lesperance, MM
Citation: In. Bespalova et al., Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss, HUM MOL GEN, 10(22), 2001, pp. 2501-2508
Substituting a telephone call for pediatric adenotonsillectomy postoperative visits
Authors: Lesperance, MM Schneider, B Garetz, SL Weatherly, RA Koopmann, CF
Citation: Mm. Lesperance et al., Substituting a telephone call for pediatric adenotonsillectomy postoperative visits, ARCH OTOLAR, 127(2), 2001, pp. 227-228
The sequence and antiapoptotic functional domains of the human cytomegalovirus UL37 exon 1 immediate early protein are conserved in multiple primary strains
Authors: Hayajneh, WA Colberg-Poley, AM Skaletskaya, A Bartle, LM Lesperance, MM Contopoulos-Ioannidis, DG Kedersha, NL Goldmacher, VS
Citation: Wa. Hayajneh et al., The sequence and antiapoptotic functional domains of the human cytomegalovirus UL37 exon 1 immediate early protein are conserved in multiple primary strains, VIROLOGY, 279(1), 2001, pp. 233-240
The carboxyl terminus of the human cytomegalovirus UL37 immediate-early glycoprotein is conserved in primary strains and is important for transactivation
Authors: Hayajneh, WA Contopoulos-Ioannidis, DG Lesperance, MM Venegas, AM Colberg-Poley, AM
Citation: Wa. Hayajneh et al., The carboxyl terminus of the human cytomegalovirus UL37 immediate-early glycoprotein is conserved in primary strains and is important for transactivation, J GEN VIROL, 82, 2001, pp. 1569-1579
DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24
Authors: Greene, CC McMillan, PM Barker, SE Kurnool, P Lomax, MI Burmeister, M Lesperance, MM
Citation: Cc. Greene et al., DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24, AM J HU GEN, 68(1), 2001, pp. 254-260
Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13
Authors: McGuirt, WT Lesperance, MM Wilcox, ER Chen, AH Van Camp, G Smith, RJH
Citation: Wt. Mcguirt et al., Characterization of autosomal dominant non-syndromic hearing loss loci: DFNA 4, 6, 10 and 13, ADV OTO-RH, 56, 2000, pp. 84-96
Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3
Authors: Lesperance, MM Burmeister, M
Citation: Mm. Lesperance et M. Burmeister, Interpretation of linkage data for a Huntington-like disorder mapping to 4p15.3, AM J HU GEN, 67(1), 2000, pp. 262-263
Pediatric myofibromatosis of the head and neck
Authors: Bech, JC Devaney, KO Weatherly, RA Koopmann, CF Lesperance, MM
Citation: Jc. Bech et al., Pediatric myofibromatosis of the head and neck, ARCH OTOLAR, 125(1), 1999, pp. 39-44
No association between DFNA6 and Pro250Arg mutation in FGFR3
Authors: Bespalova, IN Burmeister, M Lesperance, MM
Citation: In. Bespalova et al., No association between DFNA6 and Pro250Arg mutation in FGFR3, AM J MED G, 88(5), 1999, pp. 451-451
A gene for autosomal dominant hearing impairment (DFNA14) maps to a regionon chromosome 4p16.3 that does not overlap the DFNA6 locus
Authors: Van Camp, G Kunst, H Flothmann, K McGuirt, W Wauters, J Marres, H Verstreken, M Bespalova, IN Burmeister, M Van de Heyning, PH Smith, RJH Willems, PJ Cremers, CWRJ Lesperance, MM
Citation: G. Van Camp et al., A gene for autosomal dominant hearing impairment (DFNA14) maps to a regionon chromosome 4p16.3 that does not overlap the DFNA6 locus, J MED GENET, 36(7), 1999, pp. 532-536
Risultati: 1-10 |