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Volumn 69, Issue 3, 2012, Pages 322-330

Clinical significance of rare copy number variations in epilepsy: A case-control survey using microarray-based comparative genomic hybridization

(32)  Striano, Pasquale a   Coppola, Antonietta c   Paravidino, Roberta b   Malacarne, Michela b   Gimelli, Stefania p   Robbiano, Angela a   Traverso, Monica a   Pezzella, Marianna a   Belcastro, Vincenzo e   Bianchi, Amedeo f   Elia, Maurizio g   Falace, Antonio a   Gazzerro, Elisabetta a   Ferlazzo, Edoardo h,i   Freri, Elena j   Galasso, Roberta a   Gobbi, Giuseppe k   Molinatto, Cristina l   Cavani, Simona b   Zuffardi, Orsetta m   more..


Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL FEATURE; COHORT ANALYSIS; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; EPILEPSY; FEMALE; GENE DELETION; GENE DUPLICATION; GENE ENRICHMENT; GENE FREQUENCY; GENE IDENTIFICATION; GENE REARRANGEMENT; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC PARAMETERS; HUMAN; INFANT; ITALY; MAJOR CLINICAL STUDY; MALE; MENTAL DEFICIENCY; MENTAL DISEASE; MICROARRAY ANALYSIS; NEUROLOGIC DISEASE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSPECTIVE STUDY; SCHOOL CHILD;

EID: 84858602053     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2011.1999     Document Type: Article
Times cited : (67)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.