<?xml version="1.0"?>
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  <leader>00596nz  a2200217n  4500</leader>
  <controlfield tag="008">230628|||anznnbab||||||||||||||a|||||||d</controlfield>
  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="a">homoit0002864</subfield>
    <subfield code="0">https://homosaurus.org/v3/homoit0002864</subfield>
  </datafield>
  <datafield tag="040" ind1=" " ind2=" ">
    <subfield code="f">homoit</subfield>
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  <datafield tag="150" ind1=" " ind2=" ">
    <subfield code="a">Luteinizing hormone insensitivity</subfield>
  </datafield>
  <datafield tag="550" ind1=" " ind2=" ">
    <subfield code="a">Variaciones intersex</subfield>
    <subfield code="0">https://homosaurus.org/v3/homoit0000669</subfield>
  </datafield>
  <datafield tag="680" ind1=" " ind2=" ">
    <subfield code="a">People with XY chromosomes and luteinizing hormone insensitivity develop the variation Leydig cell hypoplasiae. Because people with XX chromosomes do not typically produce Leydig cells to begin with, someone with XX chromosomes who has a genetic insensitivity to luteinizing hormone will not be affected in the same way. A person with XX chromosomes whose body does not respond to luteinizing hormone will not usually have any noticeable differences at birth, but their ovaries may not produce fertile follicles (eggs), and they may not menstruate.</subfield>
  </datafield>
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