Use of repetitive DNA for diagnosis of chromosomal rearrangements
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00292365.pdf
Reference19 articles.
1. Antonarakis SE, Phillips JA III, Kazazian HH (1982) Genetic diseases: Diagnosis by restriction endonuclease analysis. J Pediatr 100:845?846
2. Borgaonkar DS (1980) Chromosomal variation in man, 35d edn. Alan R. Liss, New York
3. Caspersson T, Zech L, Johansson C (1970) Differential binding of alkylating fluorochromes in human chromosomes. Exp Cell Res 60:315?319
4. Cooke JH (1976) Repeated sequence specific to human males. Nature 262:182?186
5. Cooke HJ, Noel B (1979) Confirmation of Y/autosome translocation using recombinant DNA. Hum Genet 50:39?44
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