https://ddn.pluspedia.org/w/index.php?action=history&feed=atom&title=Fragiles_X_Syndrom 2026-08-23T00:29:39Z Versionsgeschichte dieser Seite in PlusPedia MediaWiki 1.43.3 https://ddn.pluspedia.org/w/index.php?title=Fragiles_X_Syndrom&diff=39323&oldid=prev 2010-03-28T14:12:04Z

<p>Die Seite wurde neu angelegt: „<a href="/wiki/Datei:Pptpdtjpg1.png" title="Datei:Pptpdtjpg1.png">miniatur|Entstehender Artikel</a> {| class=&quot;wikitable&quot; | | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Siehe auch&#039;&#039;&#039; | align=&quot;left&quot; width=&quot;800&quot; | |- | bgcolor=&quot;#d…“</p> <p><b>Neue Seite</b></p><div>[[Datei:pptpdtjpg1.png|miniatur|Entstehender Artikel]]<br /> {| class=&quot;wikitable&quot; |<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Siehe auch&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot; |<br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Freie Übersichtsartikel&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot; |&lt;ref name=&quot;PMID15052536&quot;&gt;The fragile-X premutation: a maturing perspective. Am J Hum Genet 74(5):805-16 (2004) PMID 15052536 &lt;/ref&gt;&lt;ref name=&quot;PMID2684038&quot;&gt;Fragile X mental retardation. Arch Dis Child 64(9):1223-4 (1989) PMID 2684038 &lt;/ref&gt;&lt;ref name=&quot;PMID11007554&quot;&gt;Dendritic spine structural anomalies in fragile-X mental retardation syndrome. Cereb Cortex 10(10):1038-44 (2000) PMID 11007554 &lt;/ref&gt;&lt;ref name=&quot;PMID18398441&quot;&gt;Fragile X syndrome. Eur J Hum Genet 16(6):666-72 (2008) PMID 18398441 &lt;/ref&gt;&lt;ref name=&quot;PMID10767313&quot;&gt;Understanding the molecular basis of fragile X syndrome. Hum Mol Genet 9(6):901-8 (2000) PMID 10767313 &lt;/ref&gt;&lt;ref name=&quot;PMID9678703&quot;&gt;The fragile X syndrome. J Med Genet 35(7):579-89 (1998) PMID 9678703 &lt;/ref&gt;&lt;ref name=&quot;PMID8100582&quot;&gt;Guidelines for the diagnosis of fragile X syndrome. National Fragile X Foundation. J Med Genet 30(5):410-3 (1993) PMID 8100582 &lt;/ref&gt;&lt;ref name=&quot;PMID1757955&quot;&gt;Molecular genetics of fragile X: a cytogenetics viewpoint. Report of the Fifth International Symposium on X Linked Mental Retardation, Strasbourg, France, 12 to 16 August 1991 (organiser Dr J-L Mandel). J Med Genet 28(12):814-7 (1991) PMID 1757955 &lt;/ref&gt;&lt;ref name=&quot;PMID1757954&quot;&gt;Cloning of the gene for the fragile X syndrome: implications for the clinical geneticist. J Med Genet 28(12):811-3 (1991) PMID 1757954 &lt;/ref&gt;&lt;ref name=&quot;PMID1757953&quot;&gt;The fragile X syndrome. J Med Genet 28(12):809-10 (1991) PMID 1757953 &lt;/ref&gt;&lt;ref name=&quot;PMID2746616&quot;&gt;Intelligence and cognitive profile in the fra(X) syndrome: a longitudinal study in 18 fra(X) boys. J Med Genet 26(7):443-6 (1989) PMID 2746616 &lt;/ref&gt;&lt;ref name=&quot;PMID6371234&quot;&gt;The fragile X syndrome: the patients and their chromosomes. J Med Genet 21(2):84-91 (1984) PMID 6371234 &lt;/ref&gt;&lt;ref name=&quot;PMID16822971&quot;&gt;Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond. J Neurosci 26(27):7151-5 (2006) PMID 16822971 &lt;/ref&gt;&lt;ref name=&quot;PMID19117905&quot;&gt;Advances in the treatment of fragile X syndrome. Pediatrics 123(1):378-90 (2009) PMID 19117905 &lt;/ref&gt;&lt;ref name=&quot;PMID9109330&quot;&gt;Fragile X syndrome. Molecular and clinical insights and treatment issues. West J Med 166(2):129-37 (1997) PMID 9109330 &lt;/ref&gt;<br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Wichtige Übersichtsartikel&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Medline Suchterm/ Synonyme&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#00dfdf&quot; | &#039;&#039;&#039;Was ist das&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Struktur&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Physiologie&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Knockout&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Transgen&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Mutation&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Polymorphismus&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Genexpression&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Inhibitoren&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |-<br /> | bgcolor=&quot;#dfdfdf&quot; | &#039;&#039;&#039;Agonisten&#039;&#039;&#039;<br /> | align=&quot;left&quot; width=&quot;800&quot;| <br /> |}<br /> <br /> ----<br /> <br /> == Bibliographie ==<br /> &lt;references /&gt;<br /> <br /> <br /> {{LinkWP_Miniartikel|Txt=Fragiles X Syndrom|Link=Fragiles-X-Syndrom}}</div>

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