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1
A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.
J Med Genet. 1986 Feb;23(1):40-5. doi: 10.1136/jmg.23.1.40.
2
A computer programme to calculate risk in X linked disorders using multiple marker loci.
J Med Genet. 1986 Feb;23(1):35-9. doi: 10.1136/jmg.23.1.35.
3
The estimation of recurrence risks in monogenic disorders using flanking marker loci.
J Med Genet. 1985 Feb;22(1):12-5. doi: 10.1136/jmg.22.1.12.
4
[Molecular genetic diagnosis in X chromosome-linked retinitis pigmentosa].
Klin Monbl Augenheilkd. 1987 Oct;191(4):307-9. doi: 10.1055/s-2008-1050516.
5
Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
Aust Paediatr J. 1988;24 Suppl 1:92-7.
6
DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
Ups J Med Sci Suppl. 1987;44:155-64.
7
[X-chromosomal hereditary night blindness: detection of carriers by segregation analysis with linked DNA markers].
Klin Monbl Augenheilkd. 1990 May;196(5):269-72. doi: 10.1055/s-2008-1046168.
8
[Norrie syndrome: identification of carriers by segregation analysis with flanking DNA markers].
Fortschr Ophthalmol. 1989;86(1):78-81.
9
Ocular manifestations in female carriers of X-linked disorders.
J Am Optom Assoc. 1995 Jun;66(6):352-6.
10
Genetic analysis of the fragile-X mental retardation syndrome with two flanking polymorphic DNA markers.
Proc Natl Acad Sci U S A. 1986 Feb;83(4):1016-20. doi: 10.1073/pnas.83.4.1016.
引用本文的文献
1
The population genetics of Duchenne: natural and artificial selection in Duchenne muscular dystrophy.
J Med Genet. 1986 Dec;23(6):521-30. doi: 10.1136/jmg.23.6.521.
2
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.
J Med Genet. 1987 Mar;24(3):152-9. doi: 10.1136/jmg.24.3.152.
3
A simple method for calculating risks before DNA analysis.
J Med Genet. 1988 Oct;25(10):663-8. doi: 10.1136/jmg.25.10.663.
4
Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.
Hum Genet. 1988 Jun;79(2):109-17. doi: 10.1007/BF00280547.
5
[New possibilities of heterozygote detection of hemophilia A].
Klin Wochenschr. 1987 Jan 15;65(2):92-6. doi: 10.1007/BF01745483.
6
Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.
J Med Genet. 1989 Sep;26(9):565-71. doi: 10.1136/jmg.26.9.565.
本文引用的文献
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How many polymorphic genes will it take to span the human genome?
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The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
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Strategies for multilocus linkage analysis in humans.
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3443-6. doi: 10.1073/pnas.81.11.3443.
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Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.
Nucleic Acids Res. 1983 Apr 25;11(8):2303-12. doi: 10.1093/nar/11.8.2303.
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Construction of a genetic linkage map in man using restriction fragment length polymorphisms.
Am J Hum Genet. 1980 May;32(3):314-31.
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Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.
Hum Genet. 1984;67(1):6-17. doi: 10.1007/BF00270551.
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New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.
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Carrier detection in Becker muscular dystrophy using creatine kinase estimation and DNA analysis.
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