A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia von Kawamura, Rie, Kato, Takema, Miyai, Shunsuke, Suzuki, Fumihiko, Naru, Yuki, Kato, Maki, Tanaka, Keiko, Nagasaka, Miwako, Tsutsumi, Makiko, Inagaki, Hidehito, Ioroi, Tomoaki, Yoshida, Makiko, Nao, Tomoya, Conlin, Laura K, Iijima, Kazumoto, Kurahashi, Hiroki, Taniguchi-Ikeda, Mariko

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Age-related decrease of meiotic cohesins in human oocytes von Tsutsumi, Makiko, Fujiwara, Reiko, Nishizawa, Haruki, Ito, Mayuko, Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae, Kato, Takema, Fujii, Takuma, Kurahashi, Hiroki

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An aggressive systemic mastocytosis preceded by ovarian dysgerminoma von Tsutsumi, Makiko, Miura, Hiroki, Inagaki, Hidehito, Shinkai, Yasuko, Kato, Asuka, Kato, Takema, Hamada-Tsutsumi, Susumu, Tanaka, Makito, Kudo, Kazuko, Yoshikawa, Tetsushi, Kurahashi, Hiroki

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HORMAD2 is essential for synapsis surveillance during meiotic prophase via the recruitment of ATR activity von Kogo, Hiroshi, Tsutsumi, Makiko, Inagaki, Hidehito, Ohye, Tamae, Kiyonari, Hiroshi, Kurahashi, Hiroki

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HORMAD1‐dependent checkpoint/surveillance mechanism eliminates asynaptic oocytes von Kogo, Hiroshi, Tsutsumi, Makiko, Ohye, Tamae, Inagaki, Hidehito, Abe, Takaya, Kurahashi, Hiroki

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Two sequential cleavage reactions on cruciform DNA structures cause palindrome-mediated chromosomal translocations von Inagaki, Hidehito, Ohye, Tamae, Kogo, Hiroshi, Tsutsumi, Makiko, Kato, Takema, Tong, Maoqing, Emanuel, Beverly S., Kurahashi, Hiroki

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Analysis of the Origin of Double Mosaic Aneuploidy in Two Cases von Kato, Takema, Kawai, Miki, Miyai, Shunsuke, Suzuki, Fumihiko, Tsutsumi, Makiko, Mizuno, Seiji, Ikeda, Toshiro, Kurahashi, Hiroki

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Palindrome-Mediated Translocations in Humans: A New Mechanistic Model for Gross Chromosomal Rearrangements von Inagaki, Hidehito, Kato, Takema, Tsutsumi, Makiko, Ouchi, Yuya, Ohye, Tamae, Kurahashi, Hiroki

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Exonic duplication of the OTC gene by a complex rearrangement that likely occurred via a replication-based mechanism: a case report von Yokoi, Katsuyuki, Nakajima, Yoko, Inagaki, Hidehito, Tsutsumi, Makiko, Ito, Tetsuya, Kurahashi, Hiroki

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Molecular analysis of low‐level mosaicism of the IKBKG mutation using the X Chromosome Inactivation pattern in Incontinentia Pigmenti von Kawai, Miki, Kato, Takema, Tsutsumi, Makiko, Shinkai, Yasuko, Inagaki, Hidehito, Kurahashi, Hiroki

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Prevalence of Emanuel syndrome: Theoretical frequency and surveillance result von Ohye, Tamae, Inagaki, Hidehito, Kato, Takema, Tsutsumi, Makiko, Kurahashi, Hiroki

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Maple syrup urine disease due to a paracentric inversion of chr 19 that disrupts BCKDHA: A case report von Yokoi, Katsuyuki, Nakajima, Yoko, Sudo, Yuta, Mariya, Tasuku, Kawamura, Rie, Tsutsumi, Makiko, Inagaki, Hidehito, Yoshikawa, Tetsushi, Ito, Tetsuya, Kurahashi, Hiroki

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Potential role for nectin-4 in the pathogenesis of pre-eclampsia: a molecular genetic study von Ito, Mayuko, Nishizawa, Haruki, Tsutsumi, Makiko, Kato, Asuka, Sakabe, Yoshiko, Noda, Yoshiteru, Ohwaki, Akiko, Miyazaki, Jun, Kato, Takema, Shiogama, Kazuya, Sekiya, Takao, Kurahashi, Hiroki, Fujii, Takuma

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A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report von Tsutsumi, Makiko, Hattori, Hiroyoshi, Akita, Nobuhiro, Maeda, Naoko, Kubota, Toshinobu, Horibe, Keizo, Fujita, Naoko, Kawai, Miki, Shinkai, Yasuko, Kato, Maki, Kato, Takema, Kawamura, Rie, Suzuki, Fumihiko, Kurahashi, Hiroki

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DEAD-box protein Ddx46 is required for the development of the digestive organs and brain in zebrafish von Hozumi, Shunya, Hirabayashi, Ryo, Yoshizawa, Akio, Ogata, Mitsuko, Ishitani, Tohru, Tsutsumi, Makiko, Kuroiwa, Atsushi, Itoh, Motoyuki, Kikuchi, Yutaka

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TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis von Yokoi, Setsuri, Ishihara, Naoko, Miya, Fuyuki, Tsutsumi, Makiko, Yanagihara, Itaru, Fujita, Naoko, Yamamoto, Hiroyuki, Kato, Mitsuhiro, Okamoto, Nobuhiko, Tsunoda, Tatsuhiko, Yamasaki, Mami, Kanemura, Yonehiro, Kosaki, Kenjiro, Kojima, Seiji, Saitoh, Shinji, Kurahashi, Hiroki, Natsume, Jun

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Recent advance in our understanding of the molecular nature of chromosomal abnormalities von Kurahashi, Hiroki, Bolor, Hasbaira, Kato, Takema, Kogo, Hiroshi, Tsutsumi, Makiko, Inagaki, Hidehito, Ohye, Tamae

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Molecular basis of maternal age-related increase in oocyte aneuploidy von Kurahashi, Hiroki, Tsutsumi, Makiko, Nishiyama, Sachie, Kogo, Hiroshi, Inagaki, Hidehito, Ohye, Tamae

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A constitutional jumping translocation involving the Y and acrocentric chromosomes von Tsutsumi, Makiko, Fujita, Naoko, Suzuki, Fumihiko, Mishima, Takashi, Fujieda, Satoko, Watari, Michiko, Takahashi, Nobuhiro, Tonoki, Hidefumi, Moriwaka, Osamu, Endo, Toshiaki, Kurahashi, Hiroki

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Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans von Kogo, Hiroshi, Kowa-Sugiyama, Hiroe, Yamada, Kouji, Bolor, Hasbaira, Tsutsumi, Makiko, Ohye, Tamae, Inagaki, Hidehito, Taniguchi, Mariko, Toda, Tatsushi, Kurahashi, Hiroki

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