Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18

Prenatal Diagnosis

Volumn 22, Issue 2, 2002, Pages 102-104

  Lee, M H ^a   Park, S Y ^a   Kim, Y M ^a   Kim, J M ^a   Han, J Y ^b   Kim, M Y ^b   Ryu, H M ^a,b  

^a Samsung Advanced Institute of Technology (SAIT)   (South Korea)

^b Sungkyunkwan University   (South Korea)

Author keywords

Complex chromosome rearrangement (CCR); Fluorescence in situ hybridization (FISH); Prenatal diagnosis

Indexed keywords

ADULT; AMNIOTIC FLUID CELL; ARTICLE; CASE REPORT; CHROMOSOME 10; CHROMOSOME 16; CHROMOSOME 18; CHROMOSOME 5; CHROMOSOME BANDING PATTERN; CHROMOSOME REARRANGEMENT; CYTOGENETICS; FAMILIAL DISEASE; FEMALE; FETUS; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; HUMAN; KARYOTYPE 46,XX; MATERNAL AGE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SPONTANEOUS ABORTION;

ABORTION, HABITUAL; ADULT; AMNIOTIC FLUID; CELLS, CULTURED; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 5; FEMALE; GESTATIONAL AGE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MATERNAL AGE; PREGNANCY; PREGNANCY, HIGH-RISK; PRENATAL DIAGNOSIS; TRANSLOCATION, GENETIC; ULTRASONOGRAPHY, PRENATAL;

EID: 0036192056     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.224     Document Type: Article

References (11)

1. A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization
2. Three prenatal diagnosis of complex chromosome rearrangement
3. Fetal translocation between chromosome 2, 18, and 21 resolved by FISH
4. Familial complex chromosome rearrangement ascertained by in situ hybridization
5. Complex chromosomal rearrangements (CCR) and their genetic consequences
6. Complex chromosome rearrangements and congenital anomalies
7. Complex chromosome rearrangements
8. Cytogenetic analysis using quantitative, high-sensitivity fluorescence hybridization
9. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangement: Two new cases and review of the literature
10. A complex chromosome rearrangement with 10 breakpoints: Tentative assignment of the locus for Williams syndrome to 4q33-q35.1
11. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridization (FISH) shows two different unbalanced karyotypes in sibs