A 13-year cytogenetic study of spontaneous abortion: Clinical applications of testing

Australian and New Zealand Journal of Obstetrics and Gynaecology

Volumn 36, Issue 3, 1996, Pages 314-318

  Ford, Judith H ^a   Wilkin, Helen Z ^a   Thomas, Philip ^a   McCarthy, Christina ^a  

^a Genetic Consulting and Testing   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ANEUPLOIDY; ARTICLE; BLOOD ANALYSIS; CHROMOSOME ANALYSIS; CHROMOSOME LOSS; COST EFFECTIVENESS ANALYSIS; CYTOGENETICS; EMBRYO; ENVIRONMENTAL FACTOR; FIRST TRIMESTER PREGNANCY; GENETICS; HUMAN; HUMAN CELL; KARYOTYPE; MAJOR CLINICAL STUDY; MATERNAL AGE; MONOSOMY X; MOSAICISM; PRIORITY JOURNAL; SPONTANEOUS ABORTION; TRISOMY; TRISOMY 16; TRISOMY 22;

EID: 0029781601     PISSN: 00048666     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1479-828X.1996.tb02719.x     Document Type: Article

References (16)

1. Bond DJ, Chandley AC, Aneuploidy. Oxford University Press, 1983 pp4-15.
2. Poland BJ, Miller JR. Effect of karyotype on zygotic development. Les Accidents Chromosomiques de la Reproduction. INSERM, 1973 pp111-161.
3. Morton NE, Jacobs PA, Hassold TJ, Wu D. Matemal age in trisomy. Ann Hum Genet 1988; 52: 227-235.
4. Hassold TJ, Chiu D. Matemal age-specific rates of numerical chromosome abnormalities with special reference to trisomy. Hum Genet 1985; 70: 11-17.
5. Hassold T, Merrill M, Adkins K, Freeman S, Sherman S. Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16. Am J Hum Genet 1995; 57: 867-874.
6. Fisher JM, Harvey JF, Morton NE, Jacobs PA. Trisomy 18: Studies of the parent and cell division of origin and the effect of aberrant recombination of nondisjunction. Am J Hum Genet 1995; 56: 669-675.
7. Sherman SL, Peterson MB, Freeman SB et al. Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination. Hum Mol Genet 1994; 3: 1529-1535.
8. Macdonald M, Hassold T, Harvey J, Wang LH, Morton NE, Jacobs P. The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and the role of aberrant recombination. Hum Mol Genet 1994; 3: 1365-1371.
9. Ford JH. Induction of chromosomal errors. Lancet 1973; 1:54.
10. Shimada T, Watanabe G, Ingalls TH. Trisomies and triploidies in hamster embryos: Induction by low-pressure hypoxia and pH imbalances. Arch Environ Health 1980; 35: 101-105.
11. Juberg RC. Origin of chromosomal abnormalities: Evidence for delayed fertilization in meiotic nondisjunction. Hum Genet 1983; 64: 122-127.
12. Chandley AC. On the parental origin of de novo mutation in man. J Med Genet 1991; 28: 217-223.
13. Ford JH, Schultz CJ, Correll AT. Chromosome elimination in miconuclei: A common cause of hypoploidy. Am J Hum Genet 1988; 43: 733-740.
14. Butcher RL. Pre-ovulatory and post-ovulatory overripeness. Int J Gynaecol Obstet 1976; 14: 105-110.
15. Ford JH, MacCormac L, Hiller J. PALS (pregnancy and lifestyle study): association between occupational and environmental exposure to chemicals and reproductive outcome. Mutation Res. 1971; 313: 153-164.
16. Martin RH, Rademaker AW. The effect of age on the frequency of sperm abnormalities m normal men. Am J Hum Genet 1987; 41: 484-492.