Minisatellite polymorphisms of the SLC6A19: Susceptibility in hypertension

Primer3 on the WWW for General Users and for Biologist Programmers

Steve Rozen, Helen Skaletsky · Humana Press eBooks · 2003 · 15K citations

Engineering, Genetics, Molecular Biology +24

Tandem repeats finder: a program to analyze DNA sequences

Gary Benson · Nucleic Acids Research · 1999 · 9.4K citations

Complete sequencing and characterization of 21,243 full-length human cDNAs

Toshio Ota, Yutaka Suzuki, Tetsuo Nishikawa et al. · Nature Genetics · 2003 · 923 citations · Full text

Dna Sequencing, Natural Sciences, Sequence Analysis +7

A serotonin transporter gene intron 2 polymorphic region, correlated with affective disorders, has allele-dependent differential enhancer-like properties in the mouse embryo

Alasdair MacKenzie, John P. Quinn · Proceedings of the National Academy of Sciences · 1999 · 375 citations · Full text

Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder

Robert Kleta, Elisa Romeo, Zorica Ristic et al. · Nature Genetics · 2004 · 308 citations · Full text

Mendelian Disorder, Genetic Disorder, Cause Hartnup Disorder +7