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Results:
1-8
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Results: 8
Authors:
Campbell, C
Cucci, RA
Prasad, S
Green, GE
Edeal, JB
Galer, CE
Karniski, LP
Sheffield, VC
Smith, RJH
Citation: C. Campbell et al., Pendred syndrome, DFNB4, and PDS/SCL26A4 identification of eight novel mutations and possible genotype-phenotype correlations, HUM MUTAT, 17(5), 2001, pp. 403-411
Authors:
Cucci, RA
Prasad, S
Kelley, PM
Green, GE
Storm, K
Willocx, S
Cohn, ES
Van Camp, G
Smith, RJH
Citation: Ra. Cucci et al., The M34T allele variant of Connexin 26, GENET TEST, 4(4), 2000, pp. 335-344
Authors:
Prasad, S
Cucci, RA
Green, GE
Smith, RJH
Citation: S. Prasad et al., Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA), HUM MUTAT, 16(6), 2000, pp. 502-508
Authors:
Green, GE
Smith, RJH
Bent, JP
Cohn, ES
Citation: Ge. Green et al., Genetic testing to identify deaf newborns, J AM MED A, 284(10), 2000, pp. 1245-1245
Authors:
Green, GE
Bauman, NM
Smith, RJH
Citation: Ge. Green et al., Pathogenesis and treatment of juvenile onset recurrent respiratory papillomatosis, OTOLAR CLIN, 33(1), 2000, pp. 187
Authors:
Jun, AI
McGuirt, WT
Hinojosa, R
Green, GE
Fischel-Ghodsian, N
Smith, RJH
Citation: Ai. Jun et al., Temporal bone histopathology in connexin 26-related hearing loss, LARYNGOSCOP, 110(2), 2000, pp. 269-275
Authors:
McGuirt, WT
Prasad, SD
Griffith, AJ
Kunst, HPM
Green, GE
Shpargel, KB
Runge, C
Huybrechts, C
Mueller, RF
Lynch, E
King, MC
Brunner, HG
Cremers, CWRJ
Takanosu, M
Li, SW
Arita, M
Mayne, R
Prockop, DJ
Van Camp, G
Smith, RJH
Citation: Wt. Mcguirt et al., Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13), NAT GENET, 23(4), 1999, pp. 413-419
Authors:
Green, GE
Scott, DA
McDonald, JM
Woodworth, GG
Sheffield, VC
Smith, RJH
Citation: Ge. Green et al., Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness, J AM MED A, 281(23), 1999, pp. 2211-2216
Risultati:
1-8
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