17932962

Source:http://linkedlifedata.com/resource/pubmed/id/17932962

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004927, umls-concept:C0016667, umls-concept:C0027816, umls-concept:C0118036, umls-concept:C0332281
pubmed:issue	1
pubmed:dateCreated	2008-2-4
pubmed:abstractText	To determine how neuroanatomic variation in children and adolescents with fragile X syndrome is linked to reduced levels of the fragile X mental retardation-1 protein and to aberrant cognition and behavior.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/EB01651, http://linkedlifedata.com/resource/pubmed/grant/HD31715, http://linkedlifedata.com/resource/pubmed/grant/K02 MH001142-09, http://linkedlifedata.com/resource/pubmed/grant/MH01142, http://linkedlifedata.com/resource/pubmed/grant/MH50047, http://linkedlifedata.com/resource/pubmed/grant/R01 MH050047-09, http://linkedlifedata.com/resource/pubmed/grant/R01 MH050047-19, http://linkedlifedata.com/resource/pubmed/grant/R21 RR019771-02, http://linkedlifedata.com/resource/pubmed/grant/RR019771
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7707449
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/FMR1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fragile X Mental Retardation Protein
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1531-8249
pubmed:author	pubmed-author:EckertMark AMA, pubmed-author:ErbaHeather WHW, pubmed-author:FurfaroJoyce AJA, pubmed-author:GolianuBrendaB, pubmed-author:GothelfDoronD, pubmed-author:HallScott SSS, pubmed-author:HayashiKiralee MKM, pubmed-author:HoeftFumikoF, pubmed-author:KraemerHelena CHC, pubmed-author:O'HaraRuthR, pubmed-author:PatnaikSwetapadmaS, pubmed-author:PivenJosephJ, pubmed-author:ReissAllan LAL, pubmed-author:RingelJessicaJ, pubmed-author:ThompsonPaul MPM
pubmed:issnType	Electronic
pubmed:volume	63
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	40-51
pubmed:dateRevised	2011-8-1
pubmed:meshHeading	pubmed-meshheading:17932962-Humans, pubmed-meshheading:17932962-Sex Factors, pubmed-meshheading:17932962-Adolescent, pubmed-meshheading:17932962-Infant, pubmed-meshheading:17932962-Brain, pubmed-meshheading:17932962-Child, pubmed-meshheading:17932962-Hypertrophy, pubmed-meshheading:17932962-Mutation, pubmed-meshheading:17932962-Child, Preschool, pubmed-meshheading:17932962-Cognition Disorders, pubmed-meshheading:17932962-Female, pubmed-meshheading:17932962-Male

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