These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
11. HLA type and islet cell antibody status in family with (diabetes insipidus and mellitus, optic atrophy, and deafness) DIDMOAD syndrome. Monson JP; Boucher BJ Lancet; 1983 Jun; 1(8336):1286-7. PubMed ID: 6134087 [No Abstract] [Full Text] [Related]
14. Diabetes insipidus, diabetes mellitus, optic atrophy and deafness. A clinical and genetic study. Nagi NA Postgrad Med J; 1979 Jun; 55(644):377-80. PubMed ID: 482181 [TBL] [Abstract][Full Text] [Related]
15. [From gene to disease; mutations in the WFS1-gene as the cause of juvenile type I diabetes mellitus with optic atrophy (Wolfram syndrome)]. Pennings RJ; Dikkeschei LD; Cremers CW; van den Ouweland JM Ned Tijdschr Geneeskd; 2002 May; 146(21):985-7. PubMed ID: 12058630 [TBL] [Abstract][Full Text] [Related]
16. [Familial syndrome of diabetes mellitus, primary optic nerve atrophy and inner-ear deafness]. Sauer H; Chüden H; Gottesbüren H; Schmitz-Valckenberg P; Seitz D Dtsch Med Wochenschr; 1973 Feb; 98(6):243-55. PubMed ID: 4684648 [No Abstract] [Full Text] [Related]