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Volumn 135, Issue 2, 2011, Pages 102-110

Clinical and molecular characterization of a combined 17p13.3 microdeletion with partial monosomy 21q21.3 in a 26-year-old man

Author keywords

Array CGH; Brain malformations; Mental retardation; Microdeletion 17pter 17p13.3; Monosomy 21pter 21q21.3

Indexed keywords

ADULT; AGYRIA; ARTICLE; BRAIN ATROPHY; BRAIN MALFORMATION; CASE REPORT; CHROMOSOME 17P; CHROMOSOME 21Q; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION 17; CHROMOSOME TRANSLOCATION 21; COMPARATIVE GENOMIC HYBRIDIZATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XY; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PARTIAL MONOSOMY; PRIORITY JOURNAL;

EID: 80054951103     PISSN: 14248581     EISSN: 14219794     Source Type: Journal    
DOI: 10.1159/000330880     Document Type: Article
Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.