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.