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The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q.
Genomics. 1997 Feb 15;40(1):48-54. doi: 10.1006/geno.1996.4541.
Genomics. 1997.
PMID: 9070918
Free article.
Two frequent missense mutations in Pendred syndrome.
Van Hauwe P, Everett LA, Coucke P, Scott DA, Kraft ML, Ris-Stalpers C, Bolder C, Otten B, de Vijlder JJ, Dietrich NL, Ramesh A, Srisailapathy SC, Parving A, Cremers CW, Willems PJ, Smith RJ, Green ED, Van Camp G.
Van Hauwe P, et al.
Hum Mol Genet. 1998 Jul;7(7):1099-104. doi: 10.1093/hmg/7.7.1099.
Hum Mol Genet. 1998.
PMID: 9618166
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Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.
Cremers CW, Admiraal RJ, Huygen PL, Bolder C, Everett LA, Joosten FB, Green ED, van Camp G, Otten BJ.
Cremers CW, et al.
Int J Pediatr Otorhinolaryngol. 1998 Oct 2;45(2):113-23. doi: 10.1016/s0165-5876(98)00123-2.
Int J Pediatr Otorhinolaryngol. 1998.
PMID: 9849679
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Progressive sensorineural hearing loss and a widened vestibular aqueduct in Pendred syndrome.
Cremers WR, Bolder C, Admiraal RJ, Everett LA, Joosten FB, van Hauwe P, Green ED, Otten BJ.
Cremers WR, et al.
Arch Otolaryngol Head Neck Surg. 1998 May;124(5):501-5. doi: 10.1001/archotol.124.5.501.
Arch Otolaryngol Head Neck Surg. 1998.
PMID: 9604973
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