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        <identifier>oai:hama-med.repo.nii.ac.jp:00002444</identifier>
        <datestamp>2023-08-02T05:05:23Z</datestamp>
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          <dc:title>Frequent Detection of Y Chromosome Sequences in Japanese Turner's Syndrome by Southern Blot Analysis of Amplified DNA</dc:title>
          <dc:creator>Nakagawa, Yuichi</dc:creator>
          <dc:creator>Natsume, Hiromune</dc:creator>
          <dc:creator>Kubota, Akira</dc:creator>
          <dc:creator>Takeuchi, Hiromi</dc:creator>
          <dc:creator>Nasuda, Kaoru</dc:creator>
          <dc:creator>Toya, Kazuhiko</dc:creator>
          <dc:creator>Endou, Akira</dc:creator>
          <dc:creator>Saegusa, Hirokazu</dc:creator>
          <dc:creator>Takeuchi, Rika</dc:creator>
          <dc:creator>Ogawa, Haruo</dc:creator>
          <dc:creator>Igarashi, Yoshio</dc:creator>
          <dc:subject>Turner syndrome,</dc:subject>
          <dc:subject>Y chromosome,</dc:subject>
          <dc:subject>PCR,</dc:subject>
          <dc:subject>Southern blot</dc:subject>
          <dc:description>In Turner's syndrome, the detection of Y chromosome sequences is very important because the presence of the Y chromosome increases the risk of gonadoblastoma induction. Some recent studies have indicated the presence of the Y chromosome in patients with Turner's syndrome, by methods in which the Y chromosome was not detected by a standard cytogenetic method, but these studies concentrated on a part of the Y chromosome or used an insensitive methods. In this study, we approached the detection of Y chromosome sequences by a sensitive method, polymerase chain reaction (PCR) with seven pairs of primers that span the Y chromosome, followed by Southern blot analysis, in eleven Japanese patients with Turner's syndrome. Ten of the eleven patients had some Y chromosome sequences determined by PCR followed by Southern blot. This suggests that most patients with Turner's syndrome have cryptic Y chromosomes, but further studies and long-term follow-up of patients with the Y chromosome are needed to support our data and to clarify the significance of a small amount of Y chromosome.</dc:description>
          <dc:description>journal article</dc:description>
          <dc:publisher>日本小児内分泌学会</dc:publisher>
          <dc:date>1996</dc:date>
          <dc:type>VoR</dc:type>
          <dc:format>application/pdf</dc:format>
          <dc:identifier>Clinical Pediatric Endocrinology</dc:identifier>
          <dc:identifier>2</dc:identifier>
          <dc:identifier>5</dc:identifier>
          <dc:identifier>83</dc:identifier>
          <dc:identifier>87</dc:identifier>
          <dc:identifier>09185739</dc:identifier>
          <dc:identifier>13477358</dc:identifier>
          <dc:identifier>https://hama-med.repo.nii.ac.jp/record/2444/files/Clinical P-5-83.pdf</dc:identifier>
          <dc:identifier>http://hdl.handle.net/10271/2512</dc:identifier>
          <dc:identifier>https://hama-med.repo.nii.ac.jp/records/2444</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:relation>10.1297/cpe.5.83</dc:relation>
          <dc:rights>The Japanese Society for Pediatric Endocrinology</dc:rights>
          <dc:rights>本文データは学協会の許諾に基づきJournal Archiveから複製したものである</dc:rights>
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