<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>47</Volume>
      <Issue>7</Issue>
      <PubDate PubStatus="epublish">
        <Year>2018</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome</title>
    <FirstPage>1058</FirstPage>
    <LastPage>1060</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Reza</FirstName>
        <LastName>JAFARZADEH ESFEHANI</LastName>
        <affiliation locale="en_US">Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran	AND Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mahtab</FirstName>
        <LastName>DASTPAK</LastName>
        <affiliation locale="en_US">Dept. of Genetic, Academic Center for Education, Culture, and Research (ACECR), Mashhad, Iran 	AND Stem Cell and Regenerative Medicine Research Group, Academic Center for Education, Culture and Research (ACECR), Khorasan Razavi Branch, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Mohammad Reza</FirstName>
        <LastName>MIRINEZHAD</LastName>
        <affiliation locale="en_US">Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran	AND Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Ariane</FirstName>
        <LastName>SADR-NABAVI</LastName>
        <affiliation locale="en_US">Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran	AND Medical Genetic Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran	AND Dept. of Genetic, Academic Center for Education, Culture, and Research (ACECR), Mashhad, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2018</Year>
        <Month>07</Month>
        <Day>16</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/14062</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/14062/6056</pdf_url>
  </Article>
</Articles>
