Prenatal diagnosis in a female carrying a deletion close to the duchenne locus
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference9 articles.
1. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
2. Molecular genetics of the human X chromosome.
3. Report of the committee on the genetic constitution of the X and Y chromosomes
4. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
5. Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.
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1. Identification of duchenne muscular dystrophy genomic probe P20 constant Taq1 fragment corresponding to the EcoRV and Msp1 polymorphisms;Prenatal Diagnosis;1991-01
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