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Volumn 168, Issue 8, 2015, Pages 669-677

X-linked intellectual disability related genes disrupted by balanced X-autosome translocations

Author keywords

IL1RAPL1; Intellectual disability; KIAA2022; TSPAN7; X chromosome; ZDHHC15

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; BALANCED X AUTOSOME TRANSLOCATION; CASE REPORT; CHROMOSOME 19; CHROMOSOME 21; CHROMOSOME 3; CHROMOSOME 9; CHROMOSOME ANALYSIS; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; COGNITIVE DEFECT; CONTROLLED STUDY; FEMALE; GENE; GENE DISRUPTION; GENE EXPRESSION PROFILING; GENE FUNCTION; GENE LOCATION; GENE MAPPING; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; IL1RAPL1 GENE; INTELLECTUAL IMPAIRMENT; INTELLIGENCE QUOTIENT; KIAA2022 GENE; MRX21 GENE; MRX34 GENE; MRX58 GENE; MRX91 GENE; MRX98 GENE; NERVE CELL DIFFERENTIATION; PRIORITY JOURNAL; PROMOTER REGION; TSPAN7 GENE; WECHSLER ADULT INTELLIGENCE SCALE; WECHSLER INTELLIGENCE SCALE FOR CHILDREN; X CHROMOSOME; X CHROMOSOME LINKED DISORDER; X LINKED INTELLECTUAL DISABILITY; CHILD; CHROMOSOMAL MAPPING; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; GENETICS; X CHROMOSOMAL INHERITANCE; X LINKED MENTAL RETARDATION;

EID: 84947038257     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.32355     Document Type: Article
Times cited : (34)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.