Prenatal diagnosis of Duchenne muscular dystrophy in the Japanese population by fluorescent CA repeat polymorphisms analysis

Journal of Obstetrics and Gynaecology Research

Volumn 23, Issue 5, 1997, Pages 453-461

  Shiroshita, Yoshiko ^a   Katayama, Susumu ^a  

^a TOHO UNIVERSITY   (Japan)

Author keywords

CA repeat polymorphisms; Duchenne muscular dystrophy; Dystrophin gene; Fluorescence; Polymerase chain reaction; Prenatal diagnosis

Indexed keywords

ARTICLE; CLINICAL ARTICLE; DNA POLYMORPHISM; DUCHENNE MUSCULAR DYSTROPHY; FEMALE; FLUORESCENCE; GENE FREQUENCY; HUMAN; JAPAN; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS;

EID: 0030701551     PISSN: 13418076     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1447-0756.1997.tb00873.x     Document Type: Article

References (16)

1. Moser H. Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention. Hum Genet 1981; 66: 17-40
2. Chamberlain JS, Gibbs RA, Ranier JF, Nguyen PN, Caskey CT. Deletion screening of the Duchenne muscular dystrophy via multiplex DNA amplification. Nucleic Acids Res 1988; 16: 11141-11156
3. Beggs AH, Koenig H, Boyce FM, Kunkel LM. Detection of 98% of DMD/BMD gene detections by polymerase chain reaction. Hum Genet 1990; 86: 45-48
4. Robert RC, Cole CG, Hart KA, Bobrow M, Bentley DR. Rapid carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy. Nucleic Acids Res 1989; 17: 811
5. Katayama S, Takeshita N, Yano T, Shiroshita Y, Katagiri Y, Kubo H, Hirakawa S, Ubagai T. Prenatal diagnosis of Duchenne muscular dystrophy analysis by the polymerase chain reaction analysis. Fetal Diagn Ther 1994; 9: 379-384
6. Feener CA, Boyce FH, Kunkel LM. Rapid detection of CA polymorphisms in cloned DNA: Application to the 5′ region of the dystrophin gene. Am J Hum Genet 1991; 48: 621-627
7. Clemens PR, Fennick Ra, Chamberlain JS, Gibbs RA, de Andrade M, Chakraborty R, Casky T. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families using dinucleotide repeat polymorphism. Am J Hum Genet 1991; 49: 951-960
8. Beggs AH, Kunkel LM. A polymorphic CACA repeat in the 3′ untranslated region of dystrophin. Nucleic Acids Res 1990; 18: 1931
9. Katagiri Y, Katayama S. Influence of mosaicism on sexing of human preembryos detected by the polymerase chain reaction. J Assist Reprod Genet 1996; 13: 586-591
10. Scott C, Kogan AB, Marie D, Gitschier J. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A. N Engl J Med 1987; 317: 985-990
11. Tsukamoto H, Inui K, Fukushima H, Okada S. Allele frequencies of intragenic, and 5′ end markers of the dystrophin gene in Japanese families afflected with Duchenne or Becker muscular dystrophy . Jpn J Hum Genet 1996; 41: 391-397
12. Kondo H, Aoki K, Onodera O, Detsuka J, Tanaka H, Tsuji S. Non-carrier diagnosis of Duchenne muscular dystrophy using CA dinucleotide repeat polymorphism. Annual Report of the Research on Nervous and Mental Disorder 1992; 47-49 (in Japanese)
13. Sandra CK, Anya LR, Rita PM, Reinald T, Mayana Z, David JC, Anneke S, Patricia MS, Donald RL. Molecular characterization of further dystrophin gene microsatellites. Mol Cell Probes 1995; 9: 361-370
14. Oudet C, Hanaeuer A, Clemence P, Caskey T, Mandel JL. Two hotspots of recombination in the DMD gene correlate with the deletion prone regions. Hum Mol Genet 1992; 1: 599-603
15. Abbes S, Roberts RG, et al. Accurate assesment of intragenic recombination frequency within the Duchenne muscular dystrophy gene. Genomics 1990; 7: 602
16. Findlay I, Ray P, Quirke P, Rutherford AJ, Lilford R. Allelic drop-out and preferential amplification in single cells and human blastomeres: Implication for preimplantation diagnosis of sex and cysic fibrosis. Hum Reprod 1995; 10: 1609-1618