Detalhe da pesquisa
1.
Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patients.
Chin Med J (Engl)
; 120(1): 46-9, 2007 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-17254487
2.
[Mutation screening of the COCH gene in familial and sporadic patients with late onset nonsyndromic sensorineural hearing loss among Chinese population].
Zhonghua Yi Xue Za Zhi
; 87(44): 3107-10, 2007 Nov 27.
Artigo
em Zh
| MEDLINE | ID: mdl-18269866
3.
[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
Zhonghua Yi Xue Za Zhi
; 86(19): 1318-22, 2006 May 23.
Artigo
em Zh
| MEDLINE | ID: mdl-16796900
4.
[Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)].
Yi Chuan
; 28(12): 1489-94, 2006 Dec.
Artigo
em Zh
| MEDLINE | ID: mdl-17138532
5.
[Clinical features of a Chinese pedigree with Waardenburg syndrome type 2].
Zhonghua Yi Xue Za Zhi
; 85(38): 2686-90, 2005 Oct 12.
Artigo
em Zh
| MEDLINE | ID: mdl-16324295
6.
Clinical observation on hearing conditions of centenarians in northern district of China.
Acta Otolaryngol
; 135(5): 451-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25739867
7.
Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairment.
Chin Med J (Engl)
; 122(7): 830-3, 2009 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19493398
8.
[Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
; 40(10): 769-73, 2005 Oct.
Artigo
em Zh
| MEDLINE | ID: mdl-16408730
9.
[Phanerogenetic retrocochlear low frequency hearing loss].
Zhonghua Er Bi Yan Hou Ke Za Zhi
; 38(6): 459-64, 2003 Dec.
Artigo
em Zh
| MEDLINE | ID: mdl-15040112