The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease.
about
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosomeA three-allele restriction-fragment-length polymorphism at the hypoxanthine phosphoribosyltransferase locus in man.Recombinant DNA approach to X-linked mental retardation.2015 William Allan Award Introduction: Kay E. Davies1.
P2860
The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease.
description
1982 nî lūn-bûn
@nan
1982年の論文
@ja
1982年論文
@yue
1982年論文
@zh-hant
1982年論文
@zh-hk
1982年論文
@zh-mo
1982年論文
@zh-tw
1982年论文
@wuu
1982年论文
@zh
1982年论文
@zh-cn
name
The Mendelian inheritance of a ...... ge studies of genetic disease.
@ast
The Mendelian inheritance of a ...... ge studies of genetic disease.
@en
type
label
The Mendelian inheritance of a ...... ge studies of genetic disease.
@ast
The Mendelian inheritance of a ...... ge studies of genetic disease.
@en
prefLabel
The Mendelian inheritance of a ...... ge studies of genetic disease.
@ast
The Mendelian inheritance of a ...... ge studies of genetic disease.
@en
P2093
P356
P1433
P1476
The Mendelian inheritance of a ...... ge studies of genetic disease.
@en
P2093
P2888
P304
P356
10.1007/BF00303007
P577
1982-01-01T00:00:00Z