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Items: 9

1.

Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.

Tekin M, Oztürkmen Akay H, Fitoz S, Birnbaum S, Cengiz FB, Sennaroğlu L, Incesulu A, Yüksel Konuk EB, Hasanefendioğlu Bayrak A, Sentürk S, Cebeci I, Utine GE, Tunçbilek E, Nance WE, Duman D.

Clin Genet. 2008 Jun;73(6):554-65. doi: 10.1111/j.1399-0004.2008.01004.x. Epub 2008 Apr 22.

PMID:
18435799
2.

Congenital Deafness with Labyrinthine Aplasia, Microtia, and Microdontia.

Ordonez J, Tekin M.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2012 Sep 20.

3.

[A report of two familial cases of Michel syndrome (bilateral agenesis of the inner ear)].

Ghazli K, Merite-Drancy A, Marsot-Dupuch K, Meyer B, Jeunesse Y, Chouard CH.

Ann Otolaryngol Chir Cervicofac. 1998 Feb;115(1):29-34. Review. French.

PMID:
9765708
4.

Profound childhood deafness. Inner ear pathology.

Lindsay JR.

Ann Otol Rhinol Laryngol. 1973 Mar-Apr;82:Suppl 5:1-121. Review. No abstract available.

PMID:
4573293
5.

Congenital deformities of the inner ear: classification and aspects regarding cochlear implant surgery.

Marangos N, Aschendorff A.

Adv Otorhinolaryngol. 1997;52:52-6. Review. No abstract available.

PMID:
9042449
6.

Anomalies of the middle and inner ear.

Rodriguez K, Shah RK, Kenna M.

Otolaryngol Clin North Am. 2007 Feb;40(1):81-96, vi. Review.

PMID:
17346562
7.

The molecular genetics of inherited deafness--current knowledge and recent advances.

Hardisty RE, Fleming J, Steel KP.

J Laryngol Otol. 1998 May;112(5):432-7. Review. No abstract available.

PMID:
9747469
8.

[The challenge of congenital and hereditary diseases].

Ni D, Leng T, Dai H.

Zhonghua Er Bi Yan Hou Ke Za Zhi. 1999 Oct;34(5):268-70. Review. Chinese. No abstract available.

PMID:
12764818
9.

[Deafness].

Kosuga M, Okuyama T.

Ryoikibetsu Shokogun Shirizu. 2001;(33):535-6. Review. Japanese. No abstract available.

PMID:
11462555

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