<?xml version='1.0' encoding='utf-8'?>
<?xml-stylesheet type="text/xsl" href="/v2/static/oai2.xsl"?>
<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>2026-10-13T05:52:07Z</responseDate>
  <request identifier="oai:figshare.com:article/33472546" metadataPrefix="oai_dc" verb="GetRecord">https://api.figshare.com/v2/oai</request>
  <GetRecord>
    <record>
      <header>
        <identifier>oai:figshare.com:article/33472546</identifier>
        <datestamp>2026-09-17T10:29:32Z</datestamp>
        <setSpec>category_24514</setSpec>
        <setSpec>item_type_3</setSpec>
        <setSpec>month_year_09_2026</setSpec>
      </header>
      <metadata>
        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Clinical and genetic dataset of MINPP1-related pontocerebellar hypoplasia type 16</dc:title>
          <dc:creator>Ming LIU (24727414)</dc:creator>
          <dc:creator>Zongqi zhou (24727537)</dc:creator>
          <dc:creator>Jing Li (25012568)</dc:creator>
          <dc:creator>Leilei Yu (25012700)</dc:creator>
          <dc:creator>Chaoyi Qi (25012802)</dc:creator>
          <dc:creator>Huifeng Wang (24727532)</dc:creator>
          <dc:subject>Medical genetics (excl. cancer genetics)</dc:subject>
          <dc:subject>PCH16</dc:subject>
          <dc:subject>MINPP1</dc:subject>
          <dc:subject>pontocerebellar hypoplasia</dc:subject>
          <dc:subject>genetic variant</dc:subject>
          <dc:subject>fetal ultrasound</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;This dataset contains de-identified clinical, imaging and genetic data of a fetus with MINPP1-related pontocerebellar hypoplasia type 16 (PCH16), for the study submitted to BMC Neurology. All personal identifiable information has been removed.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-17T10:29:32Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.33472546.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Clinical_and_genetic_dataset_of_MINPP1-related_pontocerebellar_hypoplasia_type_16/33472546</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
        </oai_dc:dc>
      </metadata>
    </record>
  </GetRecord>
</OAI-PMH>
