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Genomics|March 19, 2004
A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3Kazunori Shibuya, Izumi Obayashi, Shuichi Asakawa, et al.
Human Mutation|March 17, 2010
KMeyeDB: a graphical database of mutations in genes that cause eye diseasesTakashi Kawamura, Masafumi Ohtsubo, Susumu Mitsuyama, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 12, 2004
Comparative genomics of the keratin-associated protein (KAP) gene clusters in human, chimpanzee, and baboonKazunori Shibuya, Jun Kudoh, Izumi Obayashi, et al.
Journal of Human Genetics|July 3, 2010
Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genesHiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 15, 2011
A case of aniridia with unilateral Peters anomalyMayu Sawada, Miho Sato, Akiko Hikoya, et al.
Journal of Ophthalmology|June 23, 2015
Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital AmaurosisKatsuhiro Hosono, Yuko Harada, Kentaro Kurata, et al.
Biochemical and Biophysical Research Communications|September 1, 2009
Analysis of eighteen deletion breakpoints in the parkin geneShuichi Asakawa, Nobutaka Hattori, Atsushi Shimizu, et al.
Experimental Eye Research|July 8, 2021
Identification of susceptibility loci for light-induced visual impairment in ratsKentaro Ohishi, Katsuhiro Hosono, Akira Obana, et al.
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