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.
5. Pendred syndrome and iodide transport in the thyroid. Kopp P; Pesce L; Solis-S JC Trends Endocrinol Metab; 2008 Sep; 19(7):260-8. PubMed ID: 18692402 [TBL] [Abstract][Full Text] [Related]
6. Genetics and phenomics of Pendred syndrome. Bizhanova A; Kopp P Mol Cell Endocrinol; 2010 Jun; 322(1-2):83-90. PubMed ID: 20298745 [TBL] [Abstract][Full Text] [Related]
7. Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan. Lai CC; Chiu CY; Shiao AS; Tso YC; Wu YC; Tu TY; Jap TS Metabolism; 2007 Sep; 56(9):1279-84. PubMed ID: 17697873 [TBL] [Abstract][Full Text] [Related]
8. [Pendred syndrome as a cause of familial deafness]. Benito González J; Pérez Plasencia D; Benito González F; Blanco Pérez P; Aguirre García F; Mories T; Cañizo Alvarez A Acta Otorrinolaringol Esp; 1999; 50(6):477-9. PubMed ID: 10502702 [TBL] [Abstract][Full Text] [Related]
9. The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q. Coucke P; Van Camp G; Demirhan O; Kabakkaya Y; Balemans W; Van Hauwe P; Van Agtmael T; Smith RJ; Parving A; Bolder CH; Cremers CW; Willems PJ Genomics; 1997 Feb; 40(1):48-54. PubMed ID: 9070918 [TBL] [Abstract][Full Text] [Related]
10. A pedigree with Pendred syndrome: case report and discussion on hereditary hearing loss. Hiyoshi M; Yamane H Acta Otolaryngol Suppl; 2004 Oct; (554):45-6. PubMed ID: 15513511 [TBL] [Abstract][Full Text] [Related]
15. Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss. Cama E; Alemanno MS; Bellacchio E; Santarelli R; Carella M; Zelante L; Palladino T; Inches I; di Paola F; Arslan E; Melchionda S Int J Pediatr Otorhinolaryngol; 2009 Oct; 73(10):1458-63. PubMed ID: 19615760 [TBL] [Abstract][Full Text] [Related]
17. A novel insertion-induced frameshift mutation of the SLC26A4 gene in a Korean family with Pendred syndrome. Sagong B; Seok JH; Kwon TJ; Kim UK; Lee SH; Lee KY Gene; 2012 Oct; 508(1):135-9. PubMed ID: 22884721 [TBL] [Abstract][Full Text] [Related]
18. Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment. López-Bigas N; Melchionda S; de Cid R; Grifa A; Zelante L; Govea N; Arbonés ML; Gasparini P; Estivill X Hum Mutat; 2001 Dec; 18(6):548. PubMed ID: 11748854 [TBL] [Abstract][Full Text] [Related]
19. Association of the long QT syndrome With goiter and deafness. Gritli S; Ben Salah M; Shili A; Robson CD; Ferjaoui M; Hendaoui L; Belhani A; Jilani SB; Gusella JF; Macrae CA Am J Cardiol; 2010 Mar; 105(5):681-6. PubMed ID: 20185017 [TBL] [Abstract][Full Text] [Related]
20. Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation. Masmoudi S; Charfedine I; Hmani M; Grati M; Ghorbel AM; Elgaied-Boulila A; Drira M; Hardelin JP; Ayadi H Am J Med Genet; 2000 Jan; 90(1):38-44. PubMed ID: 10602116 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]