Chromosomes, Human, 19-20

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  Subject Areas on Research

  • BrdU-33258 Hoechst analysis of DNA replication in human lymphocytes with supernumerary or structurally abnormal X chromosomes. 
  • Cytogenetic findings in congenital leukemia: case report and review of the literature. 
  • Epilepsy due to 20q13.33 subtelomere deletion masquerading as pyridoxine-dependent epilepsy. 
  • Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy. 
  • Myotonic muscular dystrophy. From clinical description to molecular genetics. 
  • RFLP identified by the anonymous DNA segment pBAM34 at 19q13.3-qter [HGM8 assignment D19S6]. 
  • RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM). 
  • Recombinant DNA strategies in genetic neurological diseases. 
  • Regional localization of the human genes for S-adenosylhomocysteine hydrolase (cen----q131) and adenosine deaminase (q131----qter) on chromosome 20. 
  • Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19.