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Results: 1-3 |
Results: 3
Complex segregation analysis of primary hepatocellular carcinoma in Chinese families: interaction of inherited susceptibility and hepatitis B viral infection.
Authors: Shen, Fu-Min Lee, Ming K. Gong, Hui-Min Cai, Xuan-Qing King, Mary-Claire
Citation: Shen, Fu-min et al., Complex segregation analysis of primary hepatocellular carcinoma in Chinese families: interaction of inherited susceptibility and hepatitis B viral infection., American journal of human genetics , 49-I(1), 1991, pp. 88-93
Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82
Authors: Walsh, Tom Shahin, Hashem Elkan-Miller, Tal Lee, Ming K. Kanaan, Moien
Citation: Walsh, Tom et al., Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82, American journal of human genetics (Online) AJHG , 87(1), 2010, pp. 90-94
Mutations in the DBP-Deficiency Protein HSD17B4 Cause Ovarian Dysgenesis, Hearing Loss, and Ataxia of Perrault Syndrome
Authors: Pierce, Sarah B. Walsh, Tom Chisholm, Karen M. Lee, Ming K. King, Mary-Claire
Citation: B. Pierce, Sarah et al., Mutations in the DBP-Deficiency Protein HSD17B4 Cause Ovarian Dysgenesis, Hearing Loss, and Ataxia of Perrault Syndrome, American journal of human genetics (Online) AJHG , 87(2), 2010, pp. 282-288
Risultati: 1-3 |