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100 related items for PubMed ID: 10359861
1. [Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness]. Yuan H, Jiang S, Yang W, Guo W, Cao J, Dai P. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Jun; 16(3):141-4. PubMed ID: 10359861 [Abstract] [Full Text] [Related]
3. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss]. Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb; 19(1):64-7. PubMed ID: 11836692 [Abstract] [Full Text] [Related]
6. [Mitochondrial DNA mutations in matrilineal nonsyndromic deafness pedigrees of southwest China]. Zhang N, Qiao X, Wang L, Liang C. Hua Xi Yi Ke Da Xue Xue Bao; 2001 Dec; 32(4):596-8, 626. PubMed ID: 12528560 [Abstract] [Full Text] [Related]
8. [Sequence analysis of mtDNA 12S rRNA, tRNA(Leu(UUR)),tRNA(Ser(UCN))and 16S rRNA gene of 12 nonsyndromic inherited deafness pedigrees]. Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Dec; 18(6):415-20. PubMed ID: 11774206 [Abstract] [Full Text] [Related]
15. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss. Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX. Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391 [Abstract] [Full Text] [Related]
18. [Analysis of mitochondrial DNA gene tRNALeu(UUR) A3243G mutation in diabetic pedigrees]. Wang CL, Li F, Hou QZ, Li HZ, Zhang Y, Ning G. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Feb 28; 26(1):74-7. PubMed ID: 19199257 [Abstract] [Full Text] [Related]
19. [Determination of the point of gene mutation in two types of tissue from the aminoglycoside antibiotics induced deaf patients]. Xu L, Chen W, Xing C. Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2001 Apr 28; 15(4):149-51. PubMed ID: 12541634 [Abstract] [Full Text] [Related]