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Author/Creator Pandya, A

3. A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. Issue 7 (1st July 2005)

Authors:
del Castillo, F J; Rodríguez-Ballesteros, M; Álvarez, A; Hutchin, T; Leonardi, E; de Oliveira, C A; Azaiez, H; Brownstein, Z; Avenarius, M R; Marlin, S; Pandya, A; Shahin, H; Siemering, K R; Weil, D; Wuyts, W; Aguirre, L A; Martín, Y; Moreno-Pelayo, M A; Villamar, M; Avraham, K B
Journal:
Journal of medical genetics
Issue:
Volume 42:Issue 7(2005)
Page Start:
588
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness. Issue 4 (1st April 2003)

Authors:
Park, H-J; Shaukat, S; Liu, X-Z; Hahn, S H; Naz, S; Ghosh, M; Kim, H-N; Moon, S-K; Abe, S; Tukamoto, K; Riazuddin, S; Kabra, M; Erdenetungalag, R; Radnaabazar, J; Khan, S; Pandya, A; Usami, S-I; Nance, W E; Wilcox, E R; Riazuddin, S
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 4(2003)
Page Start:
242
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗