Prenatal detection of structural abnormalities of chromosome 18: Associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening

Prenatal Diagnosis

Volumn 22, Issue 8, 2002, Pages 645-648

  Graf, Michael D ^a,c   Gill, Prabhcharan ^b   Krew, Michael ^b   Schwartz, Stuart ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b AULTMAN HOSPITAL   (United States)

^c Center for Human Genetics   (United States)

Author keywords

Cytogenetics; Interphase FISH; Isochromosome 18; Prenatal screening; Trisomy 18

Indexed keywords

ADULT; AMNIOCENTESIS; ARTICLE; CASE REPORT; CHROMOSOME 18; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ASSOCIATION; GENETIC SCREENING; HUMAN; INTERPHASE; ISOCHROMOSOME; MATERNAL SERUM; PRENATAL SCREENING; PRIORITY JOURNAL; SCREENING TEST; STRUCTURAL CHROMOSOME ABERRATION; TRISOMY 18; AMNION FLUID; BLOOD; CHEMISTRY; CHROMOSOME ABERRATION; CYTOLOGY; GESTATIONAL AGE; MALE; PRENATAL DIAGNOSIS; TRISOMY;

ADULT; ALPHA-FETOPROTEINS; AMNIOCENTESIS; AMNIOTIC FLUID; CASE REPORT; CHORIONIC GONADOTROPIN; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 18; ESTRIOL; FEMALE; GESTATIONAL AGE; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; INTERPHASE; ISOCHROMOSOMES; MALE; PRENATAL DIAGNOSIS; TRISOMY; HUMANS;

ALPHA FETOPROTEIN; CHORIONIC GONADOTROPIN; ESTRIOL;

EID: 0036023275     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.354     Document Type: Article

References (13)

1. Molecular mapping of the Edwards syndrome phenotype to two noncontiguous regions on chromosome 18
2. A prospective evaluation of a second-trimester screening test for fetal Down syndrome using maternal serum alpha-fetoprotein, hCG, and unconjugated estriol
3. Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient management
4. Trisomy 18 syndrome with an unusual karyotype: Possible double isochromosome
5. 46,XY,i(21q) identified by maternal serum screening
6. Trisomy 18 syndrome caused by translocation or isochromosome formation
7. Update and review: Maternal serum screening
8. The safety and efficacy of chorionic villus sampling for early prenatal diagnosis of cytogenetic abnormalities
9. Sex chromosome aneuploidy: The Denver Prospective Study
10. Trisomy 18qter and trisomy mapping of chromosome 18
11. Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: Experience in 911 prenatal cases
12. Efficiency of rapid in situ hybridization methods for prenatal diagnosis of chromosome abnormalities causing birth defects
13. Trisomy 18 and 18p- features in a case of isochromosome 18q [46,XY,i(18q)]: Prenatal diagnosis and autopsy report