7566463

Source:http://linkedlifedata.com/resource/pubmed/id/7566463

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0035372, umls-concept:C0243064, umls-concept:C0449438, umls-concept:C0521116
pubmed:issue	2
pubmed:dateCreated	1995-10-30
pubmed:abstractText	Rett syndrome is a progressive neurological development syndrome. Evidences for a genetic transmission, but no conclusive data which entirely support the X chromosome involvement, exist. The chromosomal region 11p14-pte has been investigated with polymorphic markers and genes in the region have been sequenced. No sequence divergencies were detected.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8101187
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0174-304X
pubmed:author	pubmed-author:AnvretMM, pubmed-author:ZhangZ PZP
pubmed:issnType	Print
pubmed:volume	26
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	88-9
pubmed:dateRevised	2008-1-16
pubmed:meshHeading	pubmed-meshheading:7566463-Chromosomes, Human, Pair 11, pubmed-meshheading:7566463-Humans, pubmed-meshheading:7566463-Rett Syndrome, pubmed-meshheading:7566463-Sex Factors, pubmed-meshheading:7566463-X Chromosome
pubmed:year	1995
pubmed:articleTitle	Current status of genetic research in Rett syndrome.
pubmed:affiliation	Department of Clinical Genetics, Karolinska Hospital, Stockholm, Sweden.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't