An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy von Toda, Tatsushi, Kobayashi, Kazuhiro, Nakahori, Yutaka, Miyake, Masashi, Matsumura, Kiichiro, Kondo-Iida, Eri, Nomura, Yoshiko, Segawa, Masaya, Yoshioka, Mieko, Saito, Kayoko, Osawa, Makiko, Hamano, Kenzo, Sakakihara, Youichi, Nonaka, Ikuya, Nakagome, Yasuo, Kanazawa, Ichiro, Nakamura, Yusuke, Tokunaga, Katsushi

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Sex identification of forensic specimens by polymerase chain reaction (PCR): Two alternative methods von Akane, Atsushi, Shiono, Hiroshi, Matsubara, Kazuo, Nakahori, Yutaka, Seki, Satoko, Nagafuchi, Shigeo, Yamada, Masao, Nakagome, Yasuo

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A Y-associated allele is shared among a few ethnic groups of Asia

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Intact Sex Determining Region Y (SRY) in a Patient with XY Pure Gonadal Dysgenesis and a Twin Brother von TSUTSUMI, OSAMU, IIDA, TAKU, TAKETANI, YUJI, SUGASE, MOTOYASU, NAKAHORI, YUTAKA, NAKAGOME, YASUO

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A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1) von Lagerström, Maria, Dahl, Niklas, Nakahori, Yutaka, Nakagome, Yasuo, Bäckman, Birgitta, Landegren, Ulf, Pettersson, Ulf

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Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb von TODA, T, MIYAKE, M, NAKAHORI, Y, KOBAYASHI, K, MIZUNO, K, SAITO, K, OSAWA, M, NAKAMURA, Y, KANAZAWA, I, NAKAGOME, Y, TOKUNAGA, K

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Guidelines for genetic testing von Matsuda, Ichiro, Niikawa, Norio, Sato, Kodo, Suzumori, Kaoru, Fukushima, Yoshimitsu, Fujiki, Norio, Kanazawa, Ichiro, Nakamura, Yusuke, Yonemoto, Shohei, Nakagome, Yasuo

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Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome von Toda, Tatsushi, Yoshioka, Mieko, Nakahori, Yutaka, Kanazawa, Ichiro, Nakamura, Yusuke, Nakagome, Yasuo

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Sex identification by polymerase chain reaction using X-Y homologous primer von Nakahori, Yutaka, Hamano, Koichi, Iwaya, Makoto, Nakagome, Yasuo

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A human Y-chromosome specific repeated DNA family (DYZ1) consists of a tandem array of pentanucleotides von Nakahori, Yutaka, Mitani, Kounosuke, Yamada, Masao, Nakagome, Yasuo

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46, XY Female Karyotype Containing SRY von Okada, Taisuke, Shinohara, Miwa, Yokoyama, Wakako, Koga, Makiko, Maeda, Haruko, Tomoda, Takashi, Araki, Kumiko, Kurashige, Takanobu, Nakahori, Yutaka, Nakagome, Yasuo

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Chromosomal localisation of a Y specific growth gene(s) von Ogata, T, Tomita, K, Hida, A, Matsuo, N, Nakahori, Y, Nakagome, Y

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A new approach in the evaluation of C-positive variants in man

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The CpG island of the FMR-1 gene is methylated differently among embryonic tissues: implication for prenatal diagnosis von Iida, Taku, Nakahori, Yutaka, Tsutsumi, Osamu, Taketani, Yuji, Nakagome, Yasuo

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YAC and Cosmid Contigs Encompassing the Fukuyama-Type Congenital Muscular Dystrophy (FCMD) Candidate Region on 9q31 von Miyake, Masashi, Nakahori, Yutaka, Matsushita, Ikumi, Kobayashi, Kazuhiro, Mizuno, Kunihiko, Hirai, Momoki, Kanazawa, Ichiro, Nakagome, Yasuo, Tokunaga, Katsushi, Toda, Tatsushi

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A novel nonsense mutation in the HMG box of the SRY gene in a patient with XY sex reversal von lida, Taku, Nakahori, Yutaka, Komaki, Rie, Mori, Eri, Hayashi, Nobuyoshi, Tsutsumi, Osamu, Taketani, Yuji, Nakagome, Yasuo

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Absence of fetal cells in maternal circulation at a level of 1 in 25,000 von Nakagome, Yasuo, Seki, Satoko, Nagafuchi, Shigeo, Nakahori, Yutaka, Sato, Kodo

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Silver Staining for the Analysis of Rearrangements of Human Acrocentric Chromosomes von ABE, Tatsuo, KAWAI, Keiichi, MISAWA, Shinichi, NAKAGOME, Yasuo

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Sex determination of forensic samples by dual PCR amplification of an X-Y homologous gene von Akane, Atsushi, Seki, Satoko, Shiono, Hiroshi, Nakamura, Hiroaki, Hasegawa, Masanori, Kagawa, Masato, Matsubara, Kazuo, Nakahori, Yutaka, Nagafuchi, Shigeo, Nakagome, Yasuo

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THE MAJORITY OF THE MARKER CHROMOSOMES IN JAPANESE PATIENTS WITH STIGMATA OF TURNER SYNDROME ARE DERIVED FROM Y-CHROMOSOMES von NAGAFUCHI, S, TAMURA, T, NAKAHORI, Y, TAKANO, K, NISHI, Y, IWATANI, N, KITAO, M, HORI, Y, KONDA, S, HASEGAWA, T, NUMABE, H, FUJIEDA, K, TANAKA, T, HIBI, NAKAGOME, Y

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