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    <Journal>
      <PublisherName>jmedicalcasereports</PublisherName>
      <JournalTitle>Frontiers in Medical Case Reports</JournalTitle>
      <PISSN>I</PISSN>
      <EISSN>S</EISSN>
      <Volume-Issue>Volume 2; Issue 5</Volume-Issue>
      <PartNumber/>
      <IssueTopic>Multidisciplinary</IssueTopic>
      <IssueLanguage>English</IssueLanguage>
      <Season>(Sep-Oct, 2021)</Season>
      <SpecialIssue>N</SpecialIssue>
      <SupplementaryIssue>N</SupplementaryIssue>
      <IssueOA>Y</IssueOA>
      <PubDate>
        <Year>-0001</Year>
        <Month>11</Month>
        <Day>30</Day>
      </PubDate>
      <ArticleType>Medical Case Reports</ArticleType>
      <ArticleTitle>Atypical 9p- Partial Deletion Syndrome: First Case in Mozambique</ArticleTitle>
      <SubTitle/>
      <ArticleLanguage>English</ArticleLanguage>
      <ArticleOA>Y</ArticleOA>
      <FirstPage>1</FirstPage>
      <LastPage>2</LastPage>
      <AuthorList>
        <Author>
          <FirstName>Hector Rafael Cespedes</FirstName>
          <LastName>Rodriguez</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>N</CorrespondingAuthor>
          <ORCID/>
          <FirstName>Valeria Isabel Muando</FirstName>
          <LastName>Chicamba</LastName>
          <AuthorLanguage>English</AuthorLanguage>
          <Affiliation/>
          <CorrespondingAuthor>Y</CorrespondingAuthor>
          <ORCID/>
        </Author>
      </AuthorList>
      <DOI/>
      <Abstract/>
      <AbstractLanguage>English</AbstractLanguage>
      <Keywords>9p- Partial Deletion Syndrome,Genetic Syndromes</Keywords>
      <URLs>
        <Abstract>https://www.jmedicalcasereports.org/ubijournal-v1copy/journals/abstract.php?article_id=13315&amp;title=Atypical 9p- Partial Deletion Syndrome: First Case in Mozambique</Abstract>
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      <References>
        <ReferencesarticleTitle>References</ReferencesarticleTitle>
        <ReferencesfirstPage>16</ReferencesfirstPage>
        <ReferenceslastPage>19</ReferenceslastPage>
        <References>Torres E, Monjagata N, Herreros MB, Ascurra M, Rodrand;iacute;guez S, Ayala A. Monosomand;iacute;a Parcial del Brazo Corto del Cromosoma 9. Pediatr (Asunciand;oacute;n) 2009; 36: 219–222.&#13;
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Alcaland;aacute; FC, Rodrand;iacute;guez MM, Casado IG, Bris LO, Fresno LS, Guerrero-Fernand;aacute;ndez J, Martand;iacute;nez-Frand;iacute;as ML, Bouthelier RG. Delecion 9p-. Disgenesia gonadal asociada a retraso mental. An Pediatr (Barc) 2010; 72: 210–214&#13;
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Fernand;aacute;ndez Calderand;oacute;n E, Galand;aacute;n Gand;oacute;mez E, Carbonell Pand;eacute;rez J, Sand;aacute;enz Hurtado J, Ledesma Alcand;aacute;zar M, Cardesa Garcand;iacute;a J. Diagnand;oacute;stico del sand;iacute;ndrome 9p– al nacimiento. Una nueva observaciand;oacute;n. AnPediatr (Barc) 2004; 61: 185-196.&#13;
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National organization for rare disorders. Chromosome 9, Partial Monosomy 9p. On-line consultation date 2016/06/10. https://rarediseases.org/rare-diseases/chromosome-9-partial-monosomy-9p/&#13;
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Sirisena ND, Wijetunge UK, de Silva R, Dissanayake VH. Child with deletion 9p syndrome presenting with craniofacial dysmorphism, developmental delay, and multiple congenital malformations. Case Rep Genet 2013; 2013: 785830.</References>
      </References>
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