Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification-Reference-Cited by-同舟云学术

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Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

Published:1996-04 Issue:4 Volume:12 Page:424-426
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Sheffield Val C.,Kraiem Zaki,Beck John C.,Nishimura Darryl,Stone Edwin M.,Salameh Muhamad,Sadeh Orit,Glaser Benjamin

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0496-424.pdf

Reference28 articles.

1. Pendred, V. Deaf autism and gorter. Lancet 2, 523 (1896).

2. Batsakis, J.G. & Nishiyama, R.H. Deafness with sporadic goiter: Pendred syndrome. Arch. Otolaryng. 76, 401–406 (1962).

3. Ilium, P., Kiaer, H.W., Hvidberg-Hansen, J. & Sondergaand, G. Fifteen cases of Pendred syndrome. Arch. Otolaryng. 96, 297–397 (1972).

4. Billerbeck, A.E.C., Cavaliere, H., Goldbeng, A.C., Kalil, J. & Medeiros-Neto, G. Clinical and molecular genetics studies in Pendred syndrome. Thyroid 4, 279–84 (1994).

5. Morgans, M.E. & Trotter, W.R. Association of congenital deafness with goiter the nature of the thyroid defect. Lancet 1, 607–609 (1958).

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