Molecular cytogenetic investigation of a balanced complex chromosomal rearrangement carrier ascertained through a neonate with partial trisomies of 13 and 22

American Journal of Medical Genetics, Part A

Volumn 143, Issue 13, 2007, Pages 1502-1509

  Ji, Kwon Park ^a   Jae, Ik Lee ^a   Hyun, Cheol Jo ^a   Jeong, Kyu Shin ^a   Won, Jun Choi ^a   Soon, Ae Lee ^a   Jong, Hak Lee ^a   Won, Young Paik ^a  

^a Gyeongsang National University School of Medicine   (South Korea)

Author keywords

Array comparative genomic hybridization (array CGH); Balanced complex chromosomal rearrangement (BCCR); Partial trisomy 13; Partial trisomy 22; Three color fluorescence in situ hybridization (three color FISH)

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 13; CHROMOSOME 22; CHROMOSOME 9; CHROMOSOME REARRANGEMENT; COMPARATIVE GENOMIC HYBRIDIZATION; CYTOGENETICS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HETEROZYGOTE; HUMAN; KARYOTYPE; MALFORMATION SYNDROME; NEWBORN; PARTIAL TRISOMY; PARTIAL TRISOMY 13; PARTIAL TRISOMY 22; PHENOTYPE; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HETEROZYGOTE; HETEROZYGOTE DETECTION; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PREGNANCY; TRISOMY;

EID: 34447313641     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.31782     Document Type: Article

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