A study of the origin of ‘shadow bands’ seen when typing dinucleotide repeat polymorphisms by the PCR
X.Y. Hauge(Oregon Health & Science University), M. Litt(Oregon Health & Science University)
Cited by 242
Related Papers
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
|Nature Genetics|1994|776
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
|Human Molecular Genetics|1998|447
The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.
|PubMed|1989|424
SECONDARY STRUCTURE IN RIBONUCLEIC ACIDS
|Proceedings of the National Academy of Sciences|1959|363
Molecular Genetics of Human Blue Cone Monochromacy
|Science|1989|325