https://embryology.med.unsw.edu.au/embryology/index.php?action=history&feed=atom&title=Template%3AGenetic
Template:Genetic - Revision history
2026-10-31T11:06:04Z
Revision history for this page on the wiki
MediaWiki 1.39.10
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=376675&oldid=prev
Z8600021 at 02:41, 13 April 2019
2019-04-13T02:41:13Z
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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>|-bgcolor="F5FFFA"</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>|-bgcolor="F5FFFA"</div></td></tr>
<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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: {{genetic abnormalities}} | {{maternal age}} | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | {{trisomy mosaicism}} | [[Monosomy]] | {{Fragile X}} | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{mitochondria}} | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | {{mitosis}} | [[International Classification of Diseases]] | {{genetics}}</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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: {{genetic abnormalities}} | {{maternal age}} | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | {{trisomy mosaicism}} | [[Monosomy]] | {{Fragile X}} | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{mitochondria<ins style="font-weight: bold; text-decoration: none;">}} | {{VACTERL</ins>}} | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | {{mitosis}} | [[International Classification of Diseases]] | {{genetics}}</div></td></tr>
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=374041&oldid=prev
Z8600021 at 03:39, 19 March 2019
2019-03-19T03:39:55Z
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=347088&oldid=prev
Z8600021 at 01:10, 23 July 2018
2018-07-23T01:10:25Z
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=336568&oldid=prev
Z8600021 at 01:39, 7 Mayıs 2018
2018-05-07T01:39:00Z
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=336566&oldid=prev
Z8600021 at 01:37, 7 Mayıs 2018
2018-05-07T01:37:20Z
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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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|<del style="font-weight: bold; text-decoration: none;">Introduction</del>]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | {{Fragile X}} | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | {{mitosis}} | [[International Classification of Diseases]] | <del style="font-weight: bold; text-decoration: none;">[[Molecular Development - Genetics]]</del></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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|<ins style="font-weight: bold; text-decoration: none;">Abnormal Development</ins>]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | {{Fragile X}} | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] <ins style="font-weight: bold; text-decoration: none;">| {{mitochondria}} </ins>| {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | {{mitosis}} | [[International Classification of Diseases]] | <ins style="font-weight: bold; text-decoration: none;">{{genetics}}</ins></div></td></tr>
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Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=333764&oldid=prev
Z8600021 at 12:33, 19 April 2018
2018-04-19T12:33:00Z
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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>|-bgcolor="F5FFFA"</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>|-bgcolor="F5FFFA"</div></td></tr>
<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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | {{Fragile X}} | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | <del style="font-weight: bold; text-decoration: none;">[[Cell Division - Mitosis|Mitosis]] </del>| [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | {{Fragile X}} | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | <ins style="font-weight: bold; text-decoration: none;">{{mitosis}} </ins>| [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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;"><div>|}<noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></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>|}<noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></div></td></tr>
</table>
Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=333756&oldid=prev
Z8600021 at 12:27, 19 April 2018
2018-04-19T12:27:42Z
<p></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:27, 19 April 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>|-bgcolor="F5FFFA"</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>|-bgcolor="F5FFFA"</div></td></tr>
<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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | <del style="font-weight: bold; text-decoration: none;">[[</del>Fragile X <del style="font-weight: bold; text-decoration: none;">Syndrome|Fragile X]] </del>| [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | <ins style="font-weight: bold; text-decoration: none;">{{</ins>Fragile X<ins style="font-weight: bold; text-decoration: none;">}} </ins>| [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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;"><div>|}<noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></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>|}<noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></div></td></tr>
</table>
Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=333138&oldid=prev
Z8600021 at 02:57, 18 April 2018
2018-04-18T02:57:45Z
<p></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 13:57, 18 April 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>|-bgcolor="F5FFFA"</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>|-bgcolor="F5FFFA"</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;"><div>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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>| [[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{trisomy X}} | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</div></td></tr>
<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><noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></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><ins style="font-weight: bold; text-decoration: none;">|}</ins><noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></div></td></tr>
</table>
Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=333134&oldid=prev
Z8600021 at 02:56, 18 April 2018
2018-04-18T02:56:45Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 13:56, 18 April 2018</td>
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<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>[[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{<ins style="font-weight: bold; text-decoration: none;">trisomy </ins>X}} | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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;"><div><noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></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><noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></div></td></tr>
</table>
Z8600021
https://embryology.med.unsw.edu.au/embryology/index.php?title=Template:Genetic&diff=332928&oldid=prev
Z8600021 at 02:28, 17 April 2018
2018-04-17T02:28:12Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 13:28, 17 April 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>:[[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{Trisomy X}} | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} <del style="font-weight: bold; text-decoration: none;">[[Molecular Development - Epigenetics|Epigenetics]] </del>| [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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>:[[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | {{trisomy 21}} | {{trisomy 18}} | {{trisomy 13}} | {{Trisomy X}} | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Alagille Syndrome|Alagille]] | [[Philadelphia chromosome]] | {{hydatidiform mole}} | {{epigenetics}} | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | {{meiosis}} | [[Cell Division - Mitosis|Mitosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]]</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;"><div><noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></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><noinclude>[[Category:Template]][[Category:Genetic Abnormalities]][[Category:Abnormal Development]]</noinclude></div></td></tr>
</table>
Z8600021