Showing results (2281-2290 of 3,511) with videos related to
Sort By:
Pageof 352
Journal of Human Genetics|December 23, 2006
Hereditary prosopagnosia (HPA): the first report outside the Caucasian populationIngo Kennerknecht, Nina Plümpe, Steve Edwards, et al.Journal of Human Genetics|December 2, 2008
Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean populationSung-Hee Han, Hong-Joon Park, Eun-Joo Kang, et al.Journal of Human Genetics|June 27, 2009
Allele frequencies of the ABCC11 gene for earwax phenotypes among ancient populations of Hokkaido, JapanTakehiro Sato, Tetsuya Amano, Hiroko Ono, et al.Journal of Human Genetics|April 18, 2009
Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiencySabrina Sacconi, Leonardo Salviati, Eva TrevissonJournal of Human Genetics|April 18, 2009
TC II deficiency: avoidance of false-negative molecular genetics by RNA-based investigationsJohannes Häberle, Silke Pauli, Christoph Berning, et al.Journal of Human Genetics|July 11, 2009
Association between dopaminergic genes (SLC6A3 and DRD2) and stuttering among Han ChineseJie Lan, Manshu Song, Chunhui Pan, et al.Journal of Human Genetics|July 4, 2009
Genetic variation of genes for xenobiotic-metabolizing enzymes and risk of bronchial asthma: the importance of gene-gene and gene-environment interactions for disease susceptibilityAlexey V Polonikov, Vladimir P Ivanov, Maria A SolodilovaJournal of Human Genetics|February 21, 2009
Genetic polymorphisms in estrogen metabolism and breast cancer risk in case-control studies in Japanese, Japanese Brazilians and non-Japanese BraziliansNaoki Shimada, Motoki Iwasaki, Yoshio Kasuga, et al.Journal of Human Genetics|August 16, 2008
Association and interaction analyses of NRG1 and ERBB4 genes with schizophrenia in a Japanese populationSae Shiota, Mamoru Tochigi, Hiroko Shimada, et al.Journal of Human Genetics|August 16, 2008
The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease)Tae-Joon Cho, Hyuk Ju Moon, Dae-Yeon Cho, et al.Pageof 352