17103455

Source:http://linkedlifedata.com/resource/pubmed/id/17103455

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008671, umls-concept:C0398791, umls-concept:C0678226, umls-concept:C1858460
pubmed:issue	1
pubmed:dateCreated	2006-12-27
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1552-4825
pubmed:author	pubmed-author:KroiselPeter MPM, pubmed-author:MüerAnnikaA, pubmed-author:NeitzelHaidemarieH, pubmed-author:PetekErwinE, pubmed-author:RauterLudwigL, pubmed-author:SodiaSigrunS, pubmed-author:SperlingKarlK, pubmed-author:TönniesHolgerH, pubmed-author:VaronRaymondaR, pubmed-author:WagnerKlausK, pubmed-author:ZierlerHanneloreH
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	143
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	92-4
pubmed:meshHeading	pubmed-meshheading:17103455-Adult, pubmed-meshheading:17103455-Chromosomes, Human, Pair 8, pubmed-meshheading:17103455-Female, pubmed-meshheading:17103455-Humans, pubmed-meshheading:17103455-In Situ Hybridization, Fluorescence, pubmed-meshheading:17103455-Infant, pubmed-meshheading:17103455-Karyotyping, pubmed-meshheading:17103455-Male, pubmed-meshheading:17103455-Mothers, pubmed-meshheading:17103455-Nijmegen Breakage Syndrome, pubmed-meshheading:17103455-Uniparental Disomy
pubmed:year	2007
pubmed:articleTitle	Nijmegen breakage syndrome (NBS) due to maternal isodisomy of chromosome 8.
pubmed:affiliation	Institute of Human Genetics, Charité, Humboldt University, Berlin, Germany.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't