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2000 2
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2002 3
2004 3
2024 0

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Page 1
Clinical presentation of DFNB1.
McGuirt WT, Prasad SD, Cucci RA, Green GE, Smith RJ. McGuirt WT, et al. Among authors: cucci ra. Adv Otorhinolaryngol. 2002;61:113-9. doi: 10.1159/000066821. Adv Otorhinolaryngol. 2002. PMID: 12408072 No abstract available.
The M34T allele variant of connexin 26.
Cucci RA, Prasad S, Kelley PM, Green GE, Storm K, Willocx S, Cohn ES, Van Camp G, Smith RJ. Cucci RA, et al. Genet Test. 2000;4(4):335-44. doi: 10.1089/109065700750065063. Genet Test. 2000. PMID: 11216656
A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
Cryns K, Orzan E, Murgia A, Huygen PL, Moreno F, del Castillo I, Chamberlin GP, Azaiez H, Prasad S, Cucci RA, Leonardi E, Snoeckx RL, Govaerts PJ, Van de Heyning PH, Van de Heyning CM, Smith RJ, Van Camp G. Cryns K, et al. Among authors: cucci ra. J Med Genet. 2004 Mar;41(3):147-54. doi: 10.1136/jmg.2003.013896. J Med Genet. 2004. PMID: 14985372 Free PMC article.
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment.
Van Laer L, Coucke P, Mueller RF, Caethoven G, Flothmann K, Prasad SD, Chamberlin GP, Houseman M, Taylor GR, Van de Heyning CM, Fransen E, Rowland J, Cucci RA, Smith RJ, Van Camp G. Van Laer L, et al. Among authors: cucci ra. J Med Genet. 2001 Aug;38(8):515-8. doi: 10.1136/jmg.38.8.515. J Med Genet. 2001. PMID: 11483639 Free PMC article.