NDLI: Prenatal diagnosis of Duchenne muscular dystrophy by DNA analysis.

Content Provider	Semantic Scholar
Author	Davies, K. E.
Copyright Year	1986
Abstract	Linkage studies have been carried out in 20 families segregating for Duchenne muscular dystrophy and eight prenatal diagnoses performed, including six first trimester diagnoses and one twin pregnancy. The results of the restriction fragment length polymorphism (RFLP) analysis suggest that not all the possible RFLPs need to be used and a strategy for carrier detection studies is proposed.
Starting Page	19
Ending Page	27
Page Count	9
File Format	PDF HTM / HTML
Alternate Webpage(s)	http://jmg.bmj.com/content/jmedgenet/23/6/556.full.pdf
PubMed reference number	2879927v1
Volume Number	23
Issue Number	6
Journal	Journal of medical genetics
Language	English
Access Restriction	Open
Subject Keyword	Heterozygote Detection Muscular Dystrophy Muscular Dystrophy, Duchenne Prenatal Diagnosis Restriction fragment length polymorphism efmoroctocog alfa 1 UNT Injection [Eloctate]
Content Type	Text
Resource Type	Article

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