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	1.	Association between mutations in the gap junction β4 gene and nonsyndromic hearing loss: genotype-phenotype correlation patterns. [electronic resource] by Li, Tung-Cheng Wang, Wen-Hung Li, Chuan Yang, Jiann-Jou Producer: 20150624 In: Molecular medicine reports vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss. [electronic resource] by Li, Tung-Cheng Kuan, Yu-Hsiang Ko, Tzu-Yu Li, Chuan Yang, Jiann-Jou Producer: 20150406 In: Biochemistry and cell biology = Biochimie et biologie cellulaire vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Increased (CTG/CAG)(n) lengths in myotonic dystrophy type 1 and Machado-Joseph disease genes in idiopathic azoospermia patients. [electronic resource] by Pan, Huichin Li, Yet-Young Li, Tung-Cheng Tsai, Wen-Tin Li, Shuan-Yow Hsiao, Kuang-Ming Producer: 20030107 In: Human reproduction (Oxford, England) vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss. [electronic resource] by Hong, Hui-Mei Yang, Jiann-Jou Su, Ching-Chyuan Chang, Juan-Yu Li, Tung-Cheng Li, Shuan-Yow Producer: 20100212 In: Human genetics vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)