<?xml version='1.0' encoding='UTF-8'?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
  <responseDate>2026-03-08T00:32:38Z</responseDate>
  <request verb="GetRecord" metadataPrefix="jpcoar_1.0" identifier="oai:hama-med.repo.nii.ac.jp:00002444">https://hama-med.repo.nii.ac.jp/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:hama-med.repo.nii.ac.jp:00002444</identifier>
        <datestamp>2023-08-02T05:05:23Z</datestamp>
        <setSpec>1:11</setSpec>
      </header>
      <metadata>
        <jpcoar:jpcoar xmlns:datacite="https://schema.datacite.org/meta/kernel-4/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcndl="http://ndl.go.jp/dcndl/terms/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:jpcoar="https://github.com/JPCOAR/schema/blob/master/1.0/" xmlns:oaire="http://namespace.openaire.eu/schema/oaire/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:rioxxterms="http://www.rioxx.net/schema/v2.0/rioxxterms/" xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns="https://github.com/JPCOAR/schema/blob/master/1.0/" xsi:schemaLocation="https://github.com/JPCOAR/schema/blob/master/1.0/jpcoar_scm.xsd">
          <dc:title xml:lang="en">Frequent Detection of Y Chromosome Sequences in Japanese Turner's Syndrome by Southern Blot Analysis of Amplified DNA</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName>Nakagawa, Yuichi</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Natsume, Hiromune</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Kubota, Akira</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Takeuchi, Hiromi</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Nasuda, Kaoru</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Toya, Kazuhiko</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Endou, Akira</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Saegusa, Hirokazu</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Takeuchi, Rika</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Ogawa, Haruo</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>Igarashi, Yoshio</jpcoar:creatorName>
          </jpcoar:creator>
          <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>
          <jpcoar:subject subjectScheme="Other">Turner syndrome,</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">Y chromosome,</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">PCR,</jpcoar:subject>
          <jpcoar:subject subjectScheme="Other">Southern blot</jpcoar:subject>
          <datacite:description descriptionType="Abstract">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.</datacite:description>
          <dc:publisher>日本小児内分泌学会</dc:publisher>
          <datacite:date dateType="Issued">1996</datacite:date>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_6501">journal article</dc:type>
          <oaire:version rdf:resource="http://purl.org/coar/version/c_970fb48d4fbd8a85">VoR</oaire:version>
          <jpcoar:identifier identifierType="HDL">http://hdl.handle.net/10271/2512</jpcoar:identifier>
          <jpcoar:identifier identifierType="URI">https://hama-med.repo.nii.ac.jp/records/2444</jpcoar:identifier>
          <jpcoar:relation relationType="isIdenticalTo">
            <jpcoar:relatedIdentifier identifierType="DOI">10.1297/cpe.5.83</jpcoar:relatedIdentifier>
          </jpcoar:relation>
          <jpcoar:sourceIdentifier identifierType="ISSN">09185739</jpcoar:sourceIdentifier>
          <jpcoar:sourceIdentifier identifierType="ISSN">13477358</jpcoar:sourceIdentifier>
          <jpcoar:sourceTitle>Clinical Pediatric Endocrinology</jpcoar:sourceTitle>
          <jpcoar:volume>5</jpcoar:volume>
          <jpcoar:issue>2</jpcoar:issue>
          <jpcoar:pageStart>83</jpcoar:pageStart>
          <jpcoar:pageEnd>87</jpcoar:pageEnd>
          <jpcoar:file>
            <jpcoar:URI label="Clinical P-5-83.pdf">https://hama-med.repo.nii.ac.jp/record/2444/files/Clinical P-5-83.pdf</jpcoar:URI>
            <jpcoar:mimeType>application/pdf</jpcoar:mimeType>
            <jpcoar:extent>1.9 MB</jpcoar:extent>
            <datacite:date dateType="Available">2018-08-27</datacite:date>
          </jpcoar:file>
        </jpcoar:jpcoar>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
