Molecular Diagnosis of X-Linked Disorders
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-71635-5_14
Reference30 articles.
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3. Bakker E, Bouten EJ, et al. (1986) DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure. J Med Genet 23: 573–580
4. Bakker E, Hofker HM, Goor N et al. (1985) Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet I: 655–658
5. Barrow ES, Miller CH, Reisner HM; Graham JB (1982) Genetic counselling in haemophilia by discriminant analysis 1975–1980. J Med Genet 19: 26–34
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