| Q68842500 | "Major minisatellite loci" detected by minisatellite clones 33.6 and 33.15 correspond to the cognate loci D1S111 and D7S437 |
| Q68730658 | A DNA marker for human chromosome 8 that detects alleles of differing sizes |
| Q89509813 | ALT: A Multi-Faceted Phenomenon |
| Q70559199 | Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA |
| Q40423765 | Activation of the ALT pathway for telomere maintenance can affect other sequences in the human genome. |
| Q34142619 | Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition |
| Q39433139 | Chromosomally Integrated Human Herpesvirus 6: Models of Viral Genome Release from the Telomere and Impacts on Human Health. |
| Q52356767 | Circulating tumour-derived DNA in metastatic soft tissue sarcoma. |
| Q68062252 | Clustering of hypervariable minisatellites in the proterminal regions of human autosomes |
| Q39549181 | Deficiency in DNA mismatch repair increases the rate of telomere shortening in normal human cells. |
| Q40007309 | Evidence for alternative lengthening of telomeres in liposarcomas in the absence of ALT-associated PML bodies. |
| Q36656811 | HHV-8-unrelated primary effusion-like lymphoma associated with clonal loss of inherited chromosomally-integrated human herpesvirus-6A from the telomere of chromosome 19q. |
| Q34146140 | High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: implications for telomere biology and human evolution. |
| Q89872450 | Human RAP1 specifically protects telomeres of senescent cells from DNA damage |
| Q39093058 | Human telomeres that carry an integrated copy of human herpesvirus 6 are often short and unstable, facilitating release of the viral genome from the chromosome |
| Q33490957 | Human telomeres that contain (CTAGGG)n repeats show replication dependent instability in somatic cells and the male germline |
| Q40072962 | Inherited Chromosomally Integrated Human Herpesvirus 6 Genomes Are Ancient, Intact, and Potentially Able To Reactivate from Telomeres. |
| Q67515027 | Isolation of telomere junction fragments by anchored polymerase chain reaction |
| Q40041009 | Lack of TRF2 in ALT cells causes PML-dependent p53 activation and loss of telomeric DNA. |
| Q69644347 | New C-band polymorphism in the White Park cattle of Great Britain |
| Q37098665 | Principles and recent advances in human DNA fingerprinting. |
| Q27657084 | Sequence variant (CTAGGG)n in the human telomere favors a G-quadruplex structure containing a G·C·G·C tetrad |
| Q41434648 | Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA. |
| Q34168294 | Structural gene encoding human factor XII is located at 5q33-qter. |
| Q101214317 | Telomere Instability in Lynch Syndrome Families Leads to Some Shorter Telomeres in MSH2+/- Carriers |
| Q47869139 | Telomere instability detected in sporadic colon cancers, some showing mutations in a mismatch repair gene. |
| Q37384125 | Telomere length maintenance--an ALTernative mechanism. |
| Q38759188 | Telomere maintenance in soft tissue sarcomas |
| Q71870874 | Telomeres and disease |
| Q58673457 | The CEPH consortium linkage map of human chromosome 16 |
| Q96774340 | The Circulating Nucleic Acid Characteristics of Non-Metastatic Soft Tissue Sarcoma Patients |
| Q69610398 | The gene for clotting factor 10 is mapped to 13q32----qter |
| Q47939565 | The plasticity of human telomeres demonstrated by a hypervariable telomere repeat array that is located on some copies of 16p and 16q. |
| Q40519621 | The proterminal regions and telomeres of human chromosomes. |