Human DNA polymorphisms and methods of analysis

Current Opinion in Biotechnology

Volumn 1, Issue 2, 1990, Pages 166-171

  Weber, James L ^a  

^a MARSHFIELD CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

GENETIC POLYMORPHISM; GENETICS; GENOME; GENOTYPE; HUMAN; REVIEW;

DNA; GENOME, HUMAN; GENOTYPE; HUMAN; POLYMORPHISM (GENETICS);

EID: 0025525784     PISSN: 09581669     EISSN: None     Source Type: Journal    
DOI: 10.1016/0958-1669(90)90026-H     Document Type: Article

References (39)

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3. DNA polymorphism and human disease
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5. Variable number of tandem repeat VNTR markers for human gene mapping
6. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
7. Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy
8. Hypervariability of simple sequences as a general source for polymorphic DNA markers
9. A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene
10. Amplification of human minisatellites by the polymerase chain reaction: Towards DNA fingerprinting of single cells
11. Amplification of a highly polymorphic VNTR segment by the polymerase chain reaction
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13. Two-dimensional DNA fingerprinting of human individuals
14. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
15. Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
16. A ligase-mediated gene detection technique
17. Detection of specific DNA sequences by fluorescence amplification: A color complementation assay
18. Detection of single DNA base differences by competitive oligonucleotide printing
19. Allele-specific enzymatic amplification of β-globin genomic DNA for diagnosis of sickle cell anemia
20. DNA diagnostics — molecular techniques and automation
21. Construction of a genetic linkage map in man using restriction fragment length polymorphisms
22. Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms
23. Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA
24. New approach for isolation of VNTR makers
25. Clustering of hypervariable minisatellites in the proterminal regions of human autosomes
26. The CEPH consortium linkage map of human chromosome 1
27. Five polymorphic microsatellite VNTRs on the human X chromosome
28. n polymorphisms
29. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4
30. n repeat
31. Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker
32. Kiefer-Higgins Multiplex DNA sequencing
33. Simultaneous analysis of multiple polymorphic loci using amplified sequence polymorphisms (ASPs)
34. Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction
35. Linkage mapping of the highly informative DNA Marker D215156 to human chromosome 21 using a polymorphic GT dinucleotide repeat
36. The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome
37. A high frequency of length polymorphisms in repeated sequences adjacent to Alu sequences
38. Towards construction of a high resolution map of the mouse genome using PCR-analyzed microsatellites
39. Multiple, mutations in highly conserved residues are found in mildly affected cystic fibrosis patients