<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>European Journal of Human Genetics &#8211; MBExC</title>
	<atom:link href="https://mbexc.de/category/publications-en/journal-en/european-journal-of-human-genetics-3/feed/" rel="self" type="application/rss+xml" />
	<link>https://mbexc.de</link>
	<description>Multiscale Bioimaging - Cluster of Excellence</description>
	<lastBuildDate>Mon, 24 Mar 2025 10:16:09 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	

<image>
	<url>https://mbexc.de/storage/2020/01/X-icon.png</url>
	<title>European Journal of Human Genetics &#8211; MBExC</title>
	<link>https://mbexc.de</link>
	<width>32</width>
	<height>32</height>
</image> 
	<item>
		<title>XRCC4-related microcephalic primordial dwarfism: description of a clinical series of 7 cases, phenotype expansion and new diagnostic approaches</title>
		<link>https://mbexc.de/xrcc4-related-microcephalic-primordial-dwarfism-description-of-a-clinical-series-of-7-cases-phenotype-expansion-and-new-diagnostic-approaches/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Mon, 24 Mar 2025 10:16:09 +0000</pubDate>
				<category><![CDATA[2025]]></category>
		<category><![CDATA[Publications]]></category>
		<category><![CDATA[Author]]></category>
		<category><![CDATA[Research Alliance]]></category>
		<category><![CDATA[Journal]]></category>
		<category><![CDATA[Release Date]]></category>
		<category><![CDATA[Latest Publications]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
		<category><![CDATA[European Journal of Human Genetics]]></category>
		<guid isPermaLink="false">https://mbexc.de/?p=21631</guid>

					<description><![CDATA[Cuinat S, Chatron N, Petit F, Brunelle P, Dincuff E, Aubert Mucca M, Bieth E, Schmetz A, Rieder H, Wollnik B, Kaulfuß S, Yigit G, McKeown C, Savage T, Mulligan MR, Bicknell LS, Corsten-Janssen N, Edery P, Lesca G, de Villartay JP, Putoux A]]></description>
		
		
		
			</item>
		<item>
		<title>Familial cleft tongue caused by a unique translation initiation codon variant in TP63</title>
		<link>https://mbexc.de/familial-cleft-tongue-caused-by-a-unique-translation-initiation-codon-variant-in-tp63/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Mon, 11 Oct 2021 10:46:32 +0000</pubDate>
				<category><![CDATA[Epigenetic Regulation of Gene Transcription]]></category>
		<category><![CDATA[Publications]]></category>
		<category><![CDATA[Author]]></category>
		<category><![CDATA[2021]]></category>
		<category><![CDATA[Journal]]></category>
		<category><![CDATA[Release Date]]></category>
		<category><![CDATA[Latest Publications]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
		<category><![CDATA[European Journal of Human Genetics]]></category>
		<guid isPermaLink="false">https://mbexc.de/?p=9279</guid>

					<description><![CDATA[Schmidt J, Schreiber G, Altmüller J, Thiele H, Nürnberg P, Li Y, Kaulfuß S, Funke R, Wilken B, Yigit G, Wollnik B]]></description>
		
		
		
			</item>
		<item>
		<title>A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome</title>
		<link>https://mbexc.de/de-novo-mutations-in-fbrsl1-cause-a-novel-recognizable-malformation-and-intellectual-disability-syndrome/</link>
		
		<dc:creator><![CDATA[Fritz Kobe]]></dc:creator>
		<pubDate>Mon, 01 Jun 2020 09:05:46 +0000</pubDate>
				<category><![CDATA[Mitochondrial Gene Expression]]></category>
		<category><![CDATA[Publications]]></category>
		<category><![CDATA[Author]]></category>
		<category><![CDATA[Research Alliance]]></category>
		<category><![CDATA[Journal]]></category>
		<category><![CDATA[Release Date]]></category>
		<category><![CDATA[2020]]></category>
		<category><![CDATA[Latest Publications]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
		<category><![CDATA[European Journal of Human Genetics]]></category>
		<guid isPermaLink="false">https://mbexc.de/?p=2135</guid>

					<description><![CDATA[Drivas TG, Li D, Nair D, Alaimo JT, Alders M, Altmuller J, Barakat TS, Bebin EM, Bertsch NL, Blackburn PR, Blesson A, Bouman AM, Brockmann K,
Brunelle P, Burmeister M, Cooper GM, Denecke J, ... Wollnik B, et al.]]></description>
		
		
		
			</item>
	</channel>
</rss>
