Authors:
Bassi, MT
Bergen, AAB
Bitoun, P
Charles, SJ
Clementi, M
Gosselin, R
Hurst, J
Lewis, RA
Lorenz, B
Meitinger, T
Messiaen, L
Ramesar, RS
Ballabio, A
Schiaffino, MV
Citation: Mt. Bassi et al., Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America, HUM GENET, 108(1), 2001, pp. 51-54
Authors:
Wissinger, B
Gamer, D
Jagle, H
Giorda, R
Marx, T
Mayer, S
Tippmann, S
Broghammer, M
Jurklies, B
Rosenberg, T
Jacobson, SG
Sener, EC
Tatlipinar, S
Hoyng, CB
Castellan, C
Bitoun, P
Andreasson, S
Rudolph, G
Kellner, U
Lorenz, B
Wolff, G
Verellen-Dumoulin, C
Schwartz, M
Cremers, FPM
Apfelstedt-ylla, E
Zrenner, E
Salati, R
Sharpe, LT
Kohl, S
Citation: B. Wissinger et al., CNGA3 mutations in hereditary cone photoreceptor disorders, AM J HU GEN, 69(4), 2001, pp. 722-737
Authors:
David, A
Bitoun, P
Lacombe, D
Lambert, JC
Nivelon, A
Vigneron, J
Verloes, A
Citation: A. David et al., Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes, J MED GENET, 36(8), 1999, pp. 599-603