Mapping of the serotonin 5‐HT_1Dα autoreceptor gene (HTR1D) on chromosome 1 using a silent polymorphism in the coding region

This publication has 14 references indexed in Scilit:

• Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity
  Genomics, 1993
• Optimization of the single-strand conformation polymorphism (SSCP) technique for detection of point mutations
  Human Mutation, 1993
• A Comprehensive Genetic Linkage Map of the Human Genome
  Science, 1992
• A second-generation linkage map of the human genome
  Nature, 1992
• Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptor
  Genomics, 1991
• Family History of Alcoholism in Violent Offenders and Impulsive Fire Setters
  Archives of General Psychiatry, 1989
• Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
  Proceedings of the National Academy of Sciences, 1989
• Modification of enzymatic-ally amplified DNA for the detection of point mutations
  Nucleic Acids Research, 1989
• MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations
  Genomics, 1987