21337688

Source:http://linkedlifedata.com/resource/pubmed/id/21337688

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039082, umls-concept:C0040715, umls-concept:C0599718, umls-concept:C0599813, umls-concept:C0599893, umls-concept:C1515568, umls-concept:C1522702, umls-concept:C1533148
pubmed:issue	3
pubmed:dateCreated	2011-5-13
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1552-4833
pubmed:author	pubmed-author:Al-AchkarWalidW, pubmed-author:JarjourRami ARA, pubmed-author:WafaAbdulsamadA
pubmed:issnType	Electronic
pubmed:volume	155A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	648-51
pubmed:meshHeading	pubmed-meshheading:21337688-Abnormalities, Multiple, pubmed-meshheading:21337688-Brain, pubmed-meshheading:21337688-Chromosomes, Human, pubmed-meshheading:21337688-Chromosomes, Human, Pair 12, pubmed-meshheading:21337688-Chromosomes, Human, Pair 17, pubmed-meshheading:21337688-Chromosomes, Human, Pair 18, pubmed-meshheading:21337688-Craniofacial Abnormalities, pubmed-meshheading:21337688-Dandy-Walker Syndrome, pubmed-meshheading:21337688-Facies, pubmed-meshheading:21337688-Fatal Outcome, pubmed-meshheading:21337688-Heart Septal Defects, Atrial, pubmed-meshheading:21337688-Humans, pubmed-meshheading:21337688-Infant, pubmed-meshheading:21337688-Karyotyping, pubmed-meshheading:21337688-Male, pubmed-meshheading:21337688-Tomography, X-Ray Computed, pubmed-meshheading:21337688-Translocation, Genetic
pubmed:year	2011
pubmed:articleTitle	A new case of de novo translocation (12;17;18)(q21.2;q22;q21.1) and cranio-cerebello-cardiac (3C) syndrome.
pubmed:affiliation	Human Genetics Division, Molecular Biology and Biotechnology Department, Atomic Energy Commission of Syria, Damascus, Syria. scientific@aec.org.sy
pubmed:publicationType	Journal Article, Case Reports