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Human Mutation|October 2, 2004
Novel and recurrent mutations clustered in the von Willebrand factor A domain of MATN3 in multiple epiphyseal dysplasiaAkihiko Mabuchi, Nobuhiko Haga, Koichi Maeda, et al.
Human Genome Variation|April 16, 2016
Identification of ITPA on chromosome 20 as a susceptibility gene for young-onset tuberculosisAyaka Nakauchi, Jing Hao Wong, Surakameth Mahasirimongkol, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 5, 2002
Association analysis of single nucleotide polymorphisms in cartilage-specific collagen genes with knee and hip osteoarthritis in the Japanese populationToshiyuki Ikeda, Akihiko Mabuchi, Akira Fukuda, et al.
Human Genome Variation|April 16, 2016
Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individualsXiaoxi Liu, Minae Kawashima, Taku Miyagawa, et al.
Nature Genetics|March 29, 2011
Common variation in GPC5 is associated with acquired nephrotic syndromeKoji Okamoto, Katsushi Tokunaga, Kent Doi, et al.
Human Genome Variation|April 16, 2016
Erratum: Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individualsXiaoxi Liu, Minae Kawashima, Taku Miyagawa, et al.
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