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Journal of Human Genetics|September 2, 2006
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype associationM Melin, J Klar, T Jr Gedde-Dahl, et al.Journal of Human Genetics|September 2, 2006
Novel mutation in the HSN2 gene in a Korean patient with hereditary sensory and autonomic neuropathy type 2Hyun-Jung Cho, Byoung Joon Kim, Yeon-Lim Suh, et al.Journal of Human Genetics|April 12, 2007
Gap junction coding genes and schizophrenia: a genetic association studyBranko Aleksic, Ryoko Ishihara, Nagahide Takahashi, et al.Journal of Human Genetics|May 4, 2007
Mutation of junctophilin type 2 associated with hypertrophic cardiomyopathyYoshihisa Matsushita, Toru Furukawa, Hiroshi Kasanuki, et al.Journal of Human Genetics|April 26, 2007
Genetic determination in onset age of wrist fractureDonghai Xiong, Wei Wang, Yuan Chen, et al.Journal of Human Genetics|June 15, 2007
Three novel mutations of the PAX6 gene in Japanese aniridia patientsToshio Kawano, Chunxia Wang, Yoshihiro Hotta, et al.Journal of Human Genetics|June 8, 2007
The Tol1 transposable element of the medaka fish moves in human and mouse cellsAkihiko Koga, Atsuko Shimada, Toshiya Kuroki, et al.Journal of Human Genetics|June 15, 2007
The association of Y chromosome haplogroups with spermatogenic failure in the Han ChineseChuncheng Lu, Feng Zhang, Yankai Xia, et al.Journal of Human Genetics|July 3, 2007
Association of the aspartic acid-repeat polymorphism in the asporin gene with age at onset of knee osteoarthritis in Han Chinese populationDongquan Shi, Takahiro Nakamura, Jin Dai, et al.Journal of Human Genetics|May 10, 2007
Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean womenShin-Yoon Kim, Jong-Young Lee, Ha Young Kim, et al.Pageof 352