omim.org

Online Mendelian Inheritance in Man (OMIM)

  • ️Mon Jul 18 1988

  1. Campbell, B., Campbell, N. R., Swift, S. Waardenburg syndrome: a variation of the first arch syndrome. Arch. Derm. 86: 718-724, 1962. [PubMed: 14018109] [Full Text: https://doi.org/10.1001/archderm.1962.01590120016003]

  2. Dolowitz, D. A. Personal Communication. Salt Lake City, Utah 1966.

  3. Fried, K., Feinmesser, M., Tsitsianov, J. Hearing impairment in female carriers of the sex-linked syndrome of deafness with albinism. J. Med. Genet. 6: 132-134, 1969. [PubMed: 5801459] [Full Text: https://doi.org/10.1136/jmg.6.2.132]

  4. Gorlin, R. J. Personal Communication. Minneapolis, Minn. 7/18/1988.

  5. Litvak, G., Sandkuyl, L., Ott, J., Buchris, V., Hildesheimer, M., Shiloh, Y. Localization of X-linked albinism-deafness syndrome (ADFN) to Xq by linkage with DNA markers. (Abstract) Cytogenet. Cell Genet. 46: 652, 1987.

  6. Margolis, E. A new hereditary syndrome--sex-linked deaf-mutism associated with total albinism. Acta Genet. Statist. Med. 12: 12-19, 1962. [PubMed: 14469778] [Full Text: https://doi.org/10.1159/000151176]

  7. Reed, W. B., Stone, V. M., Boder, E., Ziprkowski, L. Pigmentary disorders in association with congenital deafness. Arch. Derm. 95: 176-186, 1967. [PubMed: 6018993]

  8. Shiloh, Y., Litvak, G., Ziv, Y., Lehner, T., Sandkuyl, L., Hildesheimer, M., Buchris, V., Cremers, F. P. M., Szabo, P., White, B. N., Holden, J. J. A., Ott, J. Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.1. Am. J. Hum. Genet. 47: 20-27, 1990. [PubMed: 2349949]

  9. Shiloh, Y., Sandkuyl, L., Litvak, G., Ziv, Y., Hildesheimer, M., Buchris, V., Ott, J. Localization of X-linked albinism-deafness syndrome (ADFN) to the region Xq26.3-27.1 by linkage analysis. (Abstract) Am. J. Hum. Genet. 43: A158, 1988.

  10. Woolf, C. M. Albinism among Indians in Arizona and New Mexico. Am. J. Hum. Genet. 17: 23-35, 1965. [PubMed: 14255554]

  11. Woolf, C. M., Dolowitz, D. A., Aldous, H. E. Congenital deafness associated with piebaldness. Arch. Otolaryng. 82: 244-250, 1965. [PubMed: 14327022] [Full Text: https://doi.org/10.1001/archotol.1965.00760010246005]

  12. Ziprkowski, L., Krakowski, A., Adam, A., Costeff, H., Sade, J. Partial albinism and deaf-mutism due to a recessive sex-linked gene. Arch. Derm. 86: 530-539, 1962. [PubMed: 14003785] [Full Text: https://doi.org/10.1001/archderm.1962.01590100144027]

  13. Zlotogora, J. X-linked albinism-deafness syndrome and Waardenburg syndrome type II: a hypothesis. (Letter) Am. J. Med. Genet. 59: 386-387, 1995. [PubMed: 8599367] [Full Text: https://doi.org/10.1002/ajmg.1320590321]

  14. Zlotogora, J., Lerer, I., Bar-David, S., Ergaz, Z., Abeliovich, D. Homozygosity for Waardenburg syndrome. Am. J. Hum. Genet. 56: 1173-1178, 1995. [PubMed: 7726174]