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          <dc:identifier>https://hdl.handle.net/10776/2291</dc:identifier>
                  <dc:date>2011-08-16</dc:date>
                  <dc:language>eng</dc:language>
                  <dc:contributor>Zhang, Mark</dc:contributor>
          <dc:contributor>Arizona State University. School of Life Sciences. Center for Biology and Society. Embryo Project Encyclopedia.</dc:contributor>
          <dc:contributor>Arizona Board of Regents</dc:contributor>
                  <dc:rights>open access</dc:rights>
          <dc:rights>http://creativecommons.org/licenses/by-nc-sa/3.0/</dc:rights>
                  <dc:description>John Hilton Edwards first described the symptoms of the genetic disorder known as Trisomy 18 - one of the most common forms of trisomy, which occurs when cells have an extra copy of a chromosome, in humans - in 1960. Trisomy 18, also known as Edwards Syndrome, occurs approximately once per 6000 live births and is second in frequency only to Trisomy 21, or Down&#039;s Syndrome, as an autosomal trisomy. Trisomy 18 causes substantial developmental problems in utero.</dc:description>
                  <dc:subject>Trisomy</dc:subject>
          <dc:subject>fetus</dc:subject>
          <dc:subject>Congenital Disorders</dc:subject>
          <dc:subject>Human Development</dc:subject>
                  <dc:title>Trisomy 18 (Edwards Syndrome)</dc:title></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>
