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2. Chromosome 16-specific repetitive DNA sequences that map to chromosomal regions known to undergo breakage/rearrangement in leukemia cells. Stallings RL; Doggett NA; Okumura K; Ward DC Genomics; 1992 Jun; 13(2):332-8. PubMed ID: 1612592 [TBL] [Abstract][Full Text] [Related]
3. FISH mapping of a human chromosome 16 constitutional pericentric inversion inv(16)(p13q22) found in a large kindred. Stallings RL; Bianchi DW Am J Med Genet; 1994 Sep; 52(3):346-8. PubMed ID: 7810567 [TBL] [Abstract][Full Text] [Related]
4. A refined physical map of the long arm of human chromosome 16. Chen LZ; Harris PC; Apostolou S; Baker E; Holman K; Lane SA; Nancarrow JK; Whitmore SA; Stallings RL; Hildebrand CE Genomics; 1991 Jun; 10(2):308-12. PubMed ID: 2071140 [TBL] [Abstract][Full Text] [Related]
5. In situ hybridization mapping of human chromosome 16: evidence for a high frequency of repetitive DNA sequences. Okumura K; Menninger J; Stallings RL; Doggett NA; Ward DC Cytogenet Cell Genet; 1994; 67(1):61-7. PubMed ID: 8187555 [TBL] [Abstract][Full Text] [Related]
6. Extensive cross-homology between the long and the short arm of chromosome 16 may explain leukemic inversions and translocations. Dauwerse JG; Jumelet EA; Wessels JW; Saris JJ; Hagemeijer A; Beverstock GC; van Ommen GJ; Breuning MH Blood; 1992 Mar; 79(5):1299-304. PubMed ID: 1536953 [TBL] [Abstract][Full Text] [Related]
7. Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p. Dauwerse JG; Kievits T; Beverstock GC; van der Keur D; Smit E; Wessels HW; Hagemeijer A; Pearson PL; van Ommen GJ; Breuning MH Cytogenet Cell Genet; 1990; 53(2-3):126-8. PubMed ID: 2369839 [TBL] [Abstract][Full Text] [Related]
8. Mapping of the human GSPT1 gene, a human homolog of the yeast GST1 gene, to chromosomal band 16p13.1. Ozawa K; Murakami Y; Eki T; Yokoyama K; Soeda E; Hoshino S; Ui M; Hanaoka F Somat Cell Mol Genet; 1992 Mar; 18(2):189-94. PubMed ID: 1574740 [TBL] [Abstract][Full Text] [Related]
9. Mapping the short arm of human chromosome 16. Callen DF; Hyland VJ; Baker EG; Fratini A; Gedeon AK; Mulley JC; Fernandez KE; Breuning MH; Sutherland GR Genomics; 1989 Apr; 4(3):348-54. PubMed ID: 2714795 [TBL] [Abstract][Full Text] [Related]
10. Isolation and mapping of human chromosome 21 cosmids using a probe for RTVL-H retrovirus-like elements. Meulenbelt I; Wapenaar MC; Patterson D; Vijg J; Uitterlinden AG Genomics; 1993 Mar; 15(3):492-9. PubMed ID: 8468043 [TBL] [Abstract][Full Text] [Related]
11. Isolation and mapping of 45 NotI linking clones to chromosome 22. Sanson M; Zhang F; Demczuk S; Delattre O; DeJong P; Aurias A; Thomas G; Rouleau GA Genomics; 1993 Sep; 17(3):776-9. PubMed ID: 8244398 [TBL] [Abstract][Full Text] [Related]
12. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s). Valero MC; de Luis O; Cruces J; Pérez Jurado LA Genomics; 2000 Oct; 69(1):1-13. PubMed ID: 11013070 [TBL] [Abstract][Full Text] [Related]
13. Isolation and characterization of a DNA fragment containing various kinds of repetitive sequences located on human chromosome 21. Yao R; Patterson D; Onodera K Jpn J Hum Genet; 1993 Sep; 38(3):243-55. PubMed ID: 8260717 [TBL] [Abstract][Full Text] [Related]
14. Radiation hybrids for mapping and cloning DNA sequences of distal 16p. Ceccherini I; Matera I; Sbrana M; Di Donato A; Yin L; Romeo G Somat Cell Mol Genet; 1992 Jul; 18(4):319-24. PubMed ID: 1440054 [TBL] [Abstract][Full Text] [Related]
15. Repeated DNA sequences in the distal long arm of the human X chromosome. Müller U; Tantravahi U; Monaco A; Stroh H; Kunkel LM; Latt SA Hum Genet; 1986 Sep; 74(1):24-9. PubMed ID: 3019869 [TBL] [Abstract][Full Text] [Related]
16. High-resolution mapping of 10 unique DNA sequences to human chromosome 3 subregions by in situ hybridization. Atchison L; Atchison ML; Cannizzaro LA Cytogenet Cell Genet; 1995; 71(2):136-8. PubMed ID: 7656582 [TBL] [Abstract][Full Text] [Related]
17. Physical map of human Xq27-qter: localizing the region of the fragile X mutation. Poustka A; Dietrich A; Langenstein G; Toniolo D; Warren ST; Lehrach H Proc Natl Acad Sci U S A; 1991 Oct; 88(19):8302-6. PubMed ID: 1924290 [TBL] [Abstract][Full Text] [Related]
18. Mapping human chromosomes in somatic cell hybrids using a low-copy-number repetitive sequence. Shaw DJ; Brook JD; Brown CS; Thomas NS Somat Cell Mol Genet; 1986 Jul; 12(4):333-7. PubMed ID: 3016914 [TBL] [Abstract][Full Text] [Related]
20. Mapping of human chromosome 22 with a panel of somatic cell hybrids. Delattre O; Azambuja CJ; Aurias A; Zucman J; Peter M; Zhang F; Hors-Cayla MC; Rouleau G; Thomas G Genomics; 1991 Apr; 9(4):721-7. PubMed ID: 2037296 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]