<?xml version="1.0"?>
<Articles JournalTitle="Acta Medica Iranica">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Acta Medica Iranica</JournalTitle>
      <Issn>0044-6025</Issn>
      <Volume>36</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>1998</Year>
        <Month>06</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">CHROMOSOMAL ABNORMALITIES IN A REFERRED POPULATION: A REPORT OF 383 IRANIAN CASES</title>
    <FirstPage>64</FirstPage>
    <LastPage>69</LastPage>
    <AuthorList>
      <Author>
        <FirstName></FirstName>
        <LastName>M. T. Akbari.</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>F. Behjati.</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
      <Author>
        <FirstName></FirstName>
        <LastName>Ashtiani  M. Khaleghian</LastName>
        <affiliation locale="en_US"></affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>09</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">This report presents the cytogenetic findings (G -banded chromosomal analysis} in 383 cases referred for suspected chromosomal abnormalities because of abnormal clinical features. Chromosomal aberrations were found in 63 116.5%) of these cases, free trisomy 21 (7%) being the most common abnormality , followed by 47, XXYkaryotype (4%). The breakdown figures for each group is discussed in the text.</abstract>
    <web_url>https://acta.tums.ac.ir/index.php/acta/article/view/1744</web_url>
    <pdf_url>https://acta.tums.ac.ir/index.php/acta/article/download/1744/1737</pdf_url>
  </Article>
</Articles>
