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      <title>P1 Evolution et santé activité introduction by ZEO</title>
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      <description>Activité d&#39;introduction</description>
      <language>en-us</language>
      <pubDate>2021-11-02 08:17:28 UTC</pubDate>
      <lastBuildDate>2023-03-27 15:46:19 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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      <item>
         <title>Objectifs activité</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861015071</link>
         <description><![CDATA[<div><em>Recenser, extraire et organiser des informations </em><br><em>Communiquer dans un langage scientifique</em>&nbsp;</div>]]></description>
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         <pubDate>2021-11-02 08:21:19 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861015071</guid>
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      <item>
         <title>Sujet</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861015983</link>
         <description><![CDATA[<div><em>Serge est atteint d'une maladie génétique. Certains de ses amis lui disent que c'est la conséquence d'un patrimoine génétique hérité de ses parents, d'autres informations que cette maladie se définit à plusieurs échelles et que l'on parle d'échelles du phénotype. Serge souhaite avoir un enfant, seulement son médecin dit qu'il fait partie d'une famille à risque, et qu'à ce titre il présente un pourcentage de risque de transmission à sa descendance de cette maladie génétique.</em></div><div><strong>Serge cherche à comprendre toutes les informations qu'on lui a transmises, non pas qu'il doute mais il est preneur d'arguments pertinents plus que de « on dit ! »</strong>&nbsp;</div>]]></description>
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         <pubDate>2021-11-02 08:21:48 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861015983</guid>
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      <item>
         <title>Consigne</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861017294</link>
         <description><![CDATA[<div><strong>A partir de l'exploitation des documents du dossier, mettre en relation les informations recueillies afin de montrer à Serge que :</strong></div><div>-&nbsp; &nbsp; &nbsp; <strong>Le phénotype se définit à différentes échelles</strong></div><div>-&nbsp; &nbsp; &nbsp; <strong>Le phénotype est déterminé génétiquement</strong></div><div>-&nbsp; &nbsp; &nbsp; <strong>Le risque de développer la maladie peut être calculé au sein d'une famille.</strong></div><div><strong>Votre production finale sera un schéma fonctionnel présentant le lien entre génotype et phénotype, complet, judicieusement produit et répondant à Serge.&nbsp;</strong></div>]]></description>
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         <pubDate>2021-11-02 08:22:33 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861017294</guid>
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      <item>
         <title>Critères d&#39;évaluation</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861020764</link>
         <description><![CDATA[<div>Voir fiche méthodo/critères du schéma fonctionnel<br><br><em><del>Sélection pertinente des informations en lien avec le sujet tous les aspects du sujet sont traités /3</del></em></div><div><em><del>Sélection judicieuse et exploitation présentée de graphiques, tableaux de valeurs issus d'études scientifiques</del></em><del> /2 <br></del><em><del>Présentation sous la forme d'un « padlet » clair, complet et richement illustré /3</del></em></div><div><em><del>Présentation orale claire, audible, employé scientifiquement rigoureux</del></em><del> /2</del></div>]]></description>
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         <pubDate>2021-11-02 08:24:29 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861020764</guid>
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      <item>
         <title>Les différentes échelles du phénotype : La mucoviscidose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861026655</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:27:52 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861026655</guid>
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      <item>
         <title>Doc 1 : Les manifestations de la mucoviscidose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861027721</link>
         <description><![CDATA[<div>&nbsp;</div>]]></description>
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         <pubDate>2021-11-02 08:28:32 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861027721</guid>
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      <item>
         <title>Doc 2 Le dysfonctionnement d’une protéine membranaire à l’origine de la maladie.</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861036048</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:33:08 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861036048</guid>
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      <item>
         <title>Doc 3 : Des mutations du gène CFTR (gène codant pour la protéine CFTR) à l’origine de la maladie</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861037811</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:33:45 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861037811</guid>
      </item>
      <item>
         <title>Arbre de la famille de Serge (II4) affectée par la mucoviscidose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861038691</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:34:18 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861038691</guid>
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      <item>
         <title>Les différentes échelles du phénotype : La drépanocytose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861040038</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:35:07 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861040038</guid>
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      <item>
         <title>Doc 1 : les symptômes associés à la drépanocytose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861043298</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:37:07 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861043298</guid>
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      <item>
         <title>Doc 2 : Défauts cellulaires de la drépanocytose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861043773</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:37:27 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861043773</guid>
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      <item>
         <title>Doc 3 : Séquences nucléotidiques et peptidiques des β-globines (individu sain en haut, drépanocytaire en bas)</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861044258</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:37:44 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861044258</guid>
      </item>
      <item>
         <title>Doc 4 : Défauts moléculaires de la drépanocytose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861044965</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:38:10 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861044965</guid>
      </item>
      <item>
         <title>Arbre de la famille de Serge (II2) affectée par la drépanocytose</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861045567</link>
         <description><![CDATA[<div>En métropole, 310 cas de drépanocytose ont été identifiés parmi les 271 887 nouveau-nés qui ont bénéficié d'un dépistage (soit 34% de la population néonatale dépistée). La prévalence est ainsi de <strong>0,11% dans la population dépistée</strong>.</div>]]></description>
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         <pubDate>2021-11-02 08:38:32 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861045567</guid>
      </item>
      <item>
         <title>Les différentes échelles du phénotype : La myopathie de Duchenne</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861062407</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:46:23 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861062407</guid>
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      <item>
         <title>Les différentes échelles du phénotype : Xeroderma pigmentosum</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861062654</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:46:31 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861062654</guid>
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      <item>
         <title>Doc 1 : les symptômes associés à xeroderma pigmentosum</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861084113</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:58:58 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861084113</guid>
      </item>
      <item>
         <title>Doc 2 :  à xeroderma pigmentosum</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861085084</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:59:34 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861085084</guid>
      </item>
      <item>
         <title>Doc 3 :  à xeroderma pigmentosum</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861085545</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 08:59:52 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861085545</guid>
      </item>
      <item>
         <title>Doc 4 :  à xeroderma pigmentosum</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861086032</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:00:10 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861086032</guid>
      </item>
      <item>
         <title>Doc 5 :  Etude de la fréquence des dimères de thymine en fonction de la dose d’UV reçue chez un individu atteint et chez un individu sain</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861086904</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:00:43 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861086904</guid>
      </item>
      <item>
         <title>Doc 6 : Elimination des dimères de thymine dans les cellules saines ou malades.</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861087782</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:01:18 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861087782</guid>
      </item>
      <item>
         <title>Arbre de la famille de Serge (III4) affectée par la Xeroderma pigmentosum</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861089480</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:02:23 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861089480</guid>
      </item>
      <item>
         <title>Doc 1 : les symptômes </title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861097284</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:07:05 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861097284</guid>
      </item>
      <item>
         <title>Doc 2 : Coupe transversale d’une portion de muscle chez un individu atteint de myopathie (MO X1000)</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861097909</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:07:31 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861097909</guid>
      </item>
      <item>
         <title>Doc 3 : Une protéine à l’origine de la maladie</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861098813</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:08:02 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861098813</guid>
      </item>
      <item>
         <title>Doc 4 : Une origine génétique de la myopathie de Duchenne</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861099606</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:08:30 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861099606</guid>
      </item>
      <item>
         <title>Arbre de la famille de Serge (IV3) affectée par la myopathie de Duchenne</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861100449</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:09:02 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861100449</guid>
      </item>
      <item>
         <title>Les différentes échelles du phénotype : Le daltonisme</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861111172</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:15:12 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861111172</guid>
      </item>
      <item>
         <title>Doc 1 : John Dalton et le daltonisme.</title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861112366</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:15:51 UTC</pubDate>
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      <item>
         <title></title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861113025</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:16:12 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861113025</guid>
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      <item>
         <title></title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861113326</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:16:22 UTC</pubDate>
         <guid>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861113326</guid>
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      <item>
         <title></title>
         <author>dany_zeo</author>
         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1861113764</link>
         <description><![CDATA[]]></description>
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         <pubDate>2021-11-02 09:16:37 UTC</pubDate>
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         <title></title>
         <author>dany_zeo</author>
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         <pubDate>2021-11-02 09:16:57 UTC</pubDate>
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         <title>Doc 2 : Des gènes des pigments rétiniens répartis sur 3 chromosomes.</title>
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         <title>Doc 3 Origine génétique du daltonisme</title>
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         <title>Arbre de la famille de Serge (III5) affectée par le daltonisme </title>
         <author>dany_zeo</author>
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      <item>
         <title>Les différentes échelles du phénotype : La phénylcétonurie</title>
         <author>dany_zeo</author>
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         <pubDate>2021-11-02 09:21:54 UTC</pubDate>
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      <item>
         <title>Les différentes échelles du phénotype : L&#39;albinisme</title>
         <author>dany_zeo</author>
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         <title>Document 1 : Les symptômes de la phénylcétonurie</title>
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         <pubDate>2021-11-02 09:45:07 UTC</pubDate>
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         <title>Document 2 : Les voies de dégradation de la phénylalanine dans l’organisme</title>
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         <pubDate>2021-11-02 09:45:28 UTC</pubDate>
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         <title>Doc 1 : l&#39;albinisme </title>
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         <link>https://padlet.com/dany_zeo/hkoqztpb2g9lw54d/wish/1874011395</link>
         <description><![CDATA[<div>L'<strong>albinisme </strong>est une <strong>maladie génétique héréditaire </strong>qui touche les mammifères, les oiseaux, les poissons, les amphibiens et les reptiles. Cette pathologie (maladie) se caractérisant par un <strong>déficit (manque) de production de mélanine (protéine) </strong>pouvant aller jusqu'à l'absence totale dans l’iris et les téguments (épiderme, poils et cheveux, plumes) et <strong>cela malgré la présence normale de cellules pigmentaires</strong>.</div>]]></description>
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         <title></title>
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         <title></title>
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         <title></title>
         <author>dany_zeo</author>
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         <pubDate>2021-11-08 03:58:25 UTC</pubDate>
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         <title></title>
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         <title>Arbre de la famille de Serge (III2) affectée par l’albinisme</title>
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         <pubDate>2021-11-08 03:59:36 UTC</pubDate>
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         <title>Arbre de la famille de Serge (III3) affectée par la phénylcétonurie</title>
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