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Volumn 51, Issue 2, 2012, Pages 245-252

Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements

Author keywords

10q; ACGH; Deletion; FISH; Inv dup del(10q); Inverted duplication

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 10Q; CHROMOSOME 22; CHROMOSOME 9; CHROMOSOME BANDING PATTERN; CHROMOSOME DELETION; CHROMOSOME DISORDER; CHROMOSOME DUPLICATION; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; COMPLEX CHROMOSOMAL REARRANGEMENT; CYTOGENETICS; FACE DYSMORPHIA; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XX; SPECTRAL KARYOTYPING;

EID: 84863873803     PISSN: 10284559     EISSN: 18756263     Source Type: Journal    
DOI: 10.1016/j.tjog.2012.04.015     Document Type: Article
Times cited : (4)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.