Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
about
Chromosomal location of the co-expressed human skeletal and cardiac actin genesTranslocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locusMolecular genetics of the human X chromosome.A computer programme to calculate risk in X linked disorders using multiple marker loci.Muscular dystrophy in girls with X;autosome translocations.DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.A simple method for calculating risks before DNA analysis.Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.Human X chromosome markers and Duchenne muscular dystrophy.Genetics of neuromuscular disorders.The enzymology of skeletal muscle disorders.The female carrier of Duchenne muscular dystrophy.
P2860
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P2860
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
description
1980 nî lūn-bûn
@nan
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
1980年论文
@zh
1980年论文
@zh-cn
name
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
@en
type
label
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
@en
prefLabel
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
@en
P1476
Duchenne muscular dystrophy. Genetic aspects, carrier detection and antenatal diagnosis.
@en
P2093
P304
P356
10.1093/OXFORDJOURNALS.BMB.A071624
P577
1980-05-01T00:00:00Z