A silent allele in the locus D19S433 contained within the AmpFℓSTR® Identifiler™ PCR Amplification Kit von Tsuji, Akiko, Ishiko, Atsushi, Umehara, Takahiro, Usumoto, Yosuke, Hikiji, Wakako, Kudo, Keiko, Ikeda, Noriaki

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Examination of the usefulness of next-generation sequencing in mixed DNA samples von Momota, Fumi, Tsuji, Akiko, Ishiko, Atsushi, Ikeda, Noriaki

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Experimental studies on identification of the driver based on STR analysis von Ishiko, Atsushi, Tsuji, Akiko, Yamaguchi, Hiroki, Hayashiba, Yasuhiko, Inoue, Hiromasa, Ikeda, Noriaki

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The structure of a variant allele which is considered to be 30.3 in the STR locus D21S11 von Tsuji, Akiko, Ishiko, Atsushi, Ikeda, Noriaki

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Estimating age of humans based on telomere shortening von Tsuji, Akiko, Ishiko, Atsushi, Takasaki, Tomoya, Ikeda, Noriaki

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Analysis of a Paternity Case in which the Alleged Father was Deceased : Single Locus Mismatch von Tsuji, Akiko, Ishiko, Atsushi, Inoue, Hiromasa, Kudo, Keiko, Ikeda, Noriaki

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Unusual death of a baby: a dog attack and confirmation using human and canine STRs von Tsuji, Akiko, Ishiko, Atsushi, Kimura, Hirohisa, Nurimoto, Masanobu, Kudo, Keiko, Ikeda, Noriaki

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Maternity Testing Using Mitochondrial DNA Analysis von Tsuji, Akiko, Ishiko, Atsushi, Hirose, Maho, Takasaki, Tomoya, Ikeda, Noriaki

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Kinship analysis using DNA typing from five skeletal remains with an unusual postmortem course von Matsumura, Shusaku, Nakazono, Takehiko, Ishiko, Atsushi, Atsuchi, Masaru, Hiroshige, Kenichi, Yamaguchi, Hiroki, Kubo, Shin-ichi

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Personal identification using Y-chromosomal short tandem repeats from bodily fluids mixed with semen von Tsuji, A, Ishiko, A, Ikeda, N, Yamaguchi, H

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Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases von Kondo, Atsushi, Nagano, China, Ishiko, Shinya, Omori, Takashi, Aoto, Yuya, Rossanti, Rini, Sakakibara, Nana, Horinouchi, Tomoko, Yamamura, Tomohiko, Nagai, Sadayuki, Okada, Eri, Shima, Yuko, Nakanishi, Koichi, Ninchoji, Takeshi, Kaito, Hiroshi, Takeda, Hiroki, Nagase, Hiroaki, Morisada, Naoya, Iijima, Kazumoto, Nozu, Kandai

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Experimental Laminin 332 Mucous Membrane Pemphigoid Critically Involves C5aR1 and Reflects Clinical and Immunopathological Characteristics of the Human Disease von Heppe, Eva Nina, Tofern, Sabrina, Schulze, Franziska S., Ishiko, Akira, Shimizu, Atsushi, Sina, Christian, Zillikens, Detlef, Köhl, Jörg, Goletz, Stephanie, Schmidt, Enno

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Mutations in SERPINB7, Encoding a Member of the Serine Protease Inhibitor Superfamily, Cause Nagashima-type Palmoplantar Keratosis von Kubo, Akiharu, Shiohama, Aiko, Sasaki, Takashi, Nakabayashi, Kazuhiko, Kawasaki, Hiroshi, Atsugi, Toru, Sato, Showbu, Shimizu, Atsushi, Mikami, Shuji, Tanizaki, Hideaki, Uchiyama, Masaki, Maeda, Tatsuo, Ito, Taisuke, Sakabe, Jun-ichi, Heike, Toshio, Okuyama, Torayuki, Kosaki, Rika, Kosaki, Kenjiro, Kudoh, Jun, Hata, Kenichiro, Umezawa, Akihiro, Tokura, Yoshiki, Ishiko, Akira, Niizeki, Hironori, Kabashima, Kenji, Mitsuhashi, Yoshihiko, Amagai, Masayuki

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X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay von Rossanti, Rini, Nozu, Kandai, Fukunaga, Atsushi, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Sakakibara, Nana, Minamikawa, Shogo, Ishiko, Shinya, Aoto, Yuya, Okada, Eri, Ninchoji, Takeshi, Kato, Noritoshi, Maruyama, Shoichi, Kono, Keiji, Nishi, Shinichi, Iijima, Kazumoto, Fujii, Hideki

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Histopathological and electron microscopic study in dogs with patellar luxation and skin hyperextensibility von UEDA, Kazunori, KAWAI, Tomoyuki, SENOO, Haruki, SHIMIZU, Atsushi, ISHIKO, Akira, NAGATA, Masahiko

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Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases von Ishiko, Shinya, Horinouchi, Tomoko, Fujimaru, Rika, Shima, Yuko, Kaito, Hiroshi, Tanaka, Ryojiro, Ishimori, Shingo, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Sakakibara, Nana, Nagano, China, Yamamura, Tomohiko, Yoshimura, Momoka, Nakanishi, Koichi, Fujimura, Junya, Kamiyoshi, Naohiro, Nagase, Hiroaki, Yoshikawa, Norishige, Iijima, Kazumoto, Nozu, Kandai

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Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes von Ishiko, Shinya, Morisada, Naoya, Kondo, Atsushi, Nagai, Sadayuki, Aoto, Yuya, Okada, Eri, Rossanti, Rini, Sakakibara, Nana, Nagano, China, Horinouchi, Tomoko, Yamamura, Tomohiko, Ninchoji, Takeshi, Kaito, Hiroshi, Hamada, Riku, Shima, Yuko, Nakanishi, Koichi, Matsuo, Masafumi, Iijima, Kazumoto, Nozu, Kandai

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Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype–genotype correlation in Japanese patients with pachydermoperiostosis von Sasaki, Takashi, Niizeki, Hironori, Shimizu, Atsushi, Shiohama, Aiko, Hirakiyama, Asami, Okuyama, Torayuki, Seki, Atsuhito, Kabashima, Kenji, Otsuka, Atsushi, Ishiko, Akira, Tanese, Keiji, Miyakawa, Shun-ichi, Sakabe, Jun-ichi, Kuwahara, Masamitsu, Amagai, Masayuki, Okano, Hideyuki, Suematsu, Makoto, Kudoh, Jun

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Clinical Features and Genotype-Phenotype Correlation of Bartter Syndrome Type 1 and 2: FR-PO604 von Kondo, Atsushi, Inoki, Yuta, Ichikawa, Yuta, Tanaka, Yu, Kitakado, Hideaki, Ueda, Chika, Ishiko, Shinya, Sakakibara, Nana, Horinouchi, Tomoko, Yamamura, Tomohiko, Iijima, Kazumoto, Nozu, Kandai

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Impact of the State of Emergency during the COVID-19 Pandemic in 2020 on Asthma Exacerbations among Children in Kobe City, Japan von Yamaguchi, Hiroshi, Nozu, Kandai, Ishiko, Shinya, Kondo, Atsushi, Ninchoji, Takeshi, Nagano, China, Takeda, Hiroki, Unzaki, Ai, Ishibashi, Kazuto, Morioka, Ichiro, Nagase, Hiroaki, Iijima, Kazumoto, Ishida, Akihito

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