Publication

Bork JM, Peters LM, Riazuddin S, Bernstein SL, Ahmed ZM, Ness SL, Polomeno R, Ramesh A, Schloss M, Srisailpathy CR, Wayne S, Bellman S, Desmukh D, Ahmed Z, Khan SN, Kaloustian VM, Li XC, Lalwani A, Riazuddin S, Bitner-Glindzicz M, Nance WE, Liu XZ, Wistow G, Smith RJ, Griffith AJ, Wilcox ER, Friedman TB, Morell RJ, Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23. Am J Hum Genet68(1):26-37 2001
PubMed ID: 11090341

Records Return:  (8) Show
 
Catalog IDDescription
HD01HUMAN VARIATION PANEL - NORTHERN EUROPEAN
HD03HUMAN VARIATION PANEL - INDO PAKISTANI
HD04HUMAN VARIATION PANEL - AFRICAN AMERICAN PANEL OF 10
HD05HUMAN VARIATION PANEL - MIDDLE EASTERN (VERSION 1)
HD07HUMAN VARIATION PANEL - JAPANESE
HD08HUMAN VARIATION PANEL - MEXICAN
HD09HUMAN VARIATION PANEL - PUERTO RICAN
HD27HUMAN VARIATION PANEL - MIDDLE EASTERN (VERSION 2)