http://en.wikisage.org/w/index.php?title=Phelan_McDermid&feed=atom&action=history
Phelan McDermid - Revision history
2024-03-29T11:35:18Z
Revision history for this page on the wiki
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http://en.wikisage.org/w/index.php?title=Phelan_McDermid&diff=7266&oldid=prev
Penarc at 22:12, 25 September 2018
2018-09-25T22:12:49Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 22:12, 25 September 2018</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[nl:Syndroom van Phelan-McDermid]]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[[nl:Syndroom van Phelan-McDermid]]</div></td></tr>
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Penarc
http://en.wikisage.org/w/index.php?title=Phelan_McDermid&diff=7263&oldid=prev
Penarc: dutch
2018-09-24T18:49:04Z
<p>dutch</p>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><references/></div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><references/></div></td></tr>
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Penarc
http://en.wikisage.org/w/index.php?title=Phelan_McDermid&diff=7262&oldid=prev
Penarc at 13:17, 24 September 2018
2018-09-24T13:17:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 13:17, 24 September 2018</td>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>(PMS<ins style="font-weight: bold; text-decoration: none;"><ref>https://www.ncbi.nlm.nih.gov/books/NBK1198/</ref></ins>) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref></div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
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Penarc
http://en.wikisage.org/w/index.php?title=Phelan_McDermid&diff=7261&oldid=prev
Penarc at 13:16, 24 September 2018
2018-09-24T13:16:12Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 13:16, 24 September 2018</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref></div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;"></ins></div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974951/pdf/fnsyn-10-00011.pdf Prospects of Zinc Supplementation in Autism Spectrum Disorders and Shankopathies Such as Phelan McDermid Syndrome]</ins></div></td></tr>
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Penarc
http://en.wikisage.org/w/index.php?title=Phelan_McDermid&diff=7258&oldid=prev
Penarc: Created page with "(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndrom..."
2018-09-24T13:09:14Z
<p>Created page with "(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndrom..."</p>
<p><b>New page</b></p><div>(PMS) is a rare genetic condition caused by deletion of terminal end of chromosome 22<ref>Phelan McDermid The 22q13,3 deletion syndrome or Phelan McDermid syndrome Mol.syndromology</ref> , about 44% of people develops [[epilepsy|seizures]]<ref>DMSF</ref><br />
<references/></div>
Penarc