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	<title>Praxis für Humangenetik Wien &#187; Hauterkrankungen</title>
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	<link>http://www.medizinische-genetik.at</link>
	<description>Dr. med. Martin Gencik  Facharzt für Medizinische Genetik (Wien, A) und Humangenetik (Münster, D)</description>
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		<title>Witkop-Syndrom</title>
		<link>http://www.medizinische-genetik.at/witkop-syndrom/</link>
		<comments>http://www.medizinische-genetik.at/witkop-syndrom/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 20:48:38 +0000</pubDate>
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				<category><![CDATA[Entwicklungsstörung]]></category>
		<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[189500]]></category>
		<category><![CDATA[MSX1]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=1255</guid>
		<description><![CDATA[Name: Witkop-Syndrom / NAIL DYSPLASIA WITH HYPODONTIA/ TOOTH-AND-NAIL SYNDROME; TNS OMIM: 189500 Gen, Region: MSX1]]></description>
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		<title>Neurofibromatose Typ 1-ähnliches Syndrom</title>
		<link>http://www.medizinische-genetik.at/neurofibromatose-typ-1-ahnliches-syndrom/</link>
		<comments>http://www.medizinische-genetik.at/neurofibromatose-typ-1-ahnliches-syndrom/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 18:19:05 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[Onkologie]]></category>
		<category><![CDATA[611431]]></category>
		<category><![CDATA[Legius]]></category>
		<category><![CDATA[Neurofibromatose]]></category>
		<category><![CDATA[SPRED1]]></category>

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		<description><![CDATA[Name: Neurofibromatose Typ 1-ähnliches Syndrom / Legius Syndrom OMIM: 611431 Gen, Region: SPRED1]]></description>
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		<title>Neurofibromatose</title>
		<link>http://www.medizinische-genetik.at/neurofibromatose/</link>
		<comments>http://www.medizinische-genetik.at/neurofibromatose/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 18:17:19 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[Onkologie]]></category>
		<category><![CDATA[193520]]></category>
		<category><![CDATA[Neurofibromatose]]></category>
		<category><![CDATA[NF1]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=1103</guid>
		<description><![CDATA[Name: Neurofibromatose / Watson Syndrom OMIM: 162200, 193520 Gen, Region: NF1]]></description>
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		<item>
		<title>McCune-Albright Syndrom</title>
		<link>http://www.medizinische-genetik.at/mccune-albright-syndrom/</link>
		<comments>http://www.medizinische-genetik.at/mccune-albright-syndrom/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 14:59:33 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[Wachstumsstörungen]]></category>
		<category><![CDATA[174800]]></category>
		<category><![CDATA[GNAS]]></category>
		<category><![CDATA[McCune-Albright]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=1034</guid>
		<description><![CDATA[Name: McCune-Albright Syndrom OMIM: 174800 Gen, Region: GNAS]]></description>
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		<title>LEOPARD Syndrom</title>
		<link>http://www.medizinische-genetik.at/leopard-syndrom/</link>
		<comments>http://www.medizinische-genetik.at/leopard-syndrom/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 14:23:35 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[Herzerkrankungen]]></category>
		<category><![CDATA[Wachstumsstörungen]]></category>
		<category><![CDATA[151100]]></category>
		<category><![CDATA[611554]]></category>
		<category><![CDATA[LEOPARD]]></category>
		<category><![CDATA[PTPN11]]></category>
		<category><![CDATA[RAF1]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=1011</guid>
		<description><![CDATA[Name: LEOPARD Syndrom OMIM: 151100 / 611554 Gen, Region: PTPN11 / RAF1]]></description>
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		<title>Incontinentia pigmenti</title>
		<link>http://www.medizinische-genetik.at/incontinentia-pigmenti/</link>
		<comments>http://www.medizinische-genetik.at/incontinentia-pigmenti/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 13:41:23 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Entwicklungsstörung]]></category>
		<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[308300]]></category>
		<category><![CDATA[Bloch-Siemens]]></category>
		<category><![CDATA[IKBKG]]></category>
		<category><![CDATA[Incontinentia pigmenti]]></category>
		<category><![CDATA[melanoblastosis]]></category>
		<category><![CDATA[naevus]]></category>
		<category><![CDATA[pigmentosus]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=970</guid>
		<description><![CDATA[Name: Bloch-Siemens-Syndrom, Incontinentia pigmenti, melanoblastosis cutis und naevus pigmentosus systematicus OMIM: 308300 Gen, Region: IKBKG]]></description>
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		<title>Hermansky-Pudlak Syndrom 7</title>
		<link>http://www.medizinische-genetik.at/hermansky-pudlak-syndrom-7/</link>
		<comments>http://www.medizinische-genetik.at/hermansky-pudlak-syndrom-7/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 12:47:27 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Augenerkrankungen]]></category>
		<category><![CDATA[Gerinnungsstörungen]]></category>
		<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[203300]]></category>
		<category><![CDATA[DTNBP1]]></category>
		<category><![CDATA[Hermansky-Pudlak]]></category>
		<category><![CDATA[Hermansky-Pudlak Syndrom 7]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=919</guid>
		<description><![CDATA[Name: Hermansky-Pudlak Syndrom 7 OMIM: 203300 Gen, Region: DTNBP1]]></description>
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		<title>Hermansky-Pudlak Syndrom 3</title>
		<link>http://www.medizinische-genetik.at/hermansky-pudlak-syndrom-3/</link>
		<comments>http://www.medizinische-genetik.at/hermansky-pudlak-syndrom-3/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 12:45:59 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Augenerkrankungen]]></category>
		<category><![CDATA[Gerinnungsstörungen]]></category>
		<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[203300]]></category>
		<category><![CDATA[Hermansky-Pudlak]]></category>
		<category><![CDATA[HPS3]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=916</guid>
		<description><![CDATA[Name: Hermansky-Pudlak Syndrom 3 OMIM: 203300 Gen, Region: HPS3]]></description>
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		<item>
		<title>Hermansky-Pudlak Syndrom 1</title>
		<link>http://www.medizinische-genetik.at/hermansky-pudlak-syndrom-1/</link>
		<comments>http://www.medizinische-genetik.at/hermansky-pudlak-syndrom-1/#comments</comments>
		<pubDate>Fri, 01 Jan 2010 12:39:22 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Augenerkrankungen]]></category>
		<category><![CDATA[Gerinnungsstörungen]]></category>
		<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[203300]]></category>
		<category><![CDATA[Albinismus]]></category>
		<category><![CDATA[Blutungsneigung]]></category>
		<category><![CDATA[Ceroid]]></category>
		<category><![CDATA[Hermansky]]></category>
		<category><![CDATA[Hermansky-Pudlak]]></category>
		<category><![CDATA[HPS1]]></category>
		<category><![CDATA[Lungenfibrose]]></category>
		<category><![CDATA[Lysosomen]]></category>
		<category><![CDATA[Pudlak]]></category>

		<guid isPermaLink="false">http://www.medgene.com/medizinische-genetik/?p=914</guid>
		<description><![CDATA[Name: Hermansky-Pudlak Syndrom 1 OMIM: 203300 Gen, Region: HPS1]]></description>
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		<title>Ehlers-Danlos Syndrom</title>
		<link>http://www.medizinische-genetik.at/ehlers-danlos-syndrom/</link>
		<comments>http://www.medizinische-genetik.at/ehlers-danlos-syndrom/#comments</comments>
		<pubDate>Sat, 26 Dec 2009 22:42:50 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[Hauterkrankungen]]></category>
		<category><![CDATA[130060]]></category>
		<category><![CDATA[COL1A1]]></category>
		<category><![CDATA[COL1A2]]></category>
		<category><![CDATA[Ehlers-Danlos]]></category>

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		<description><![CDATA[Name: Ehlers-Danlos, arthrochalastischer Typ (7A u. 7B) OMIM:  130060 Gen, Region: COL1A1 / COL1A2]]></description>
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