145 related articles for article (PubMed ID: 2884625)
1. Identification of 28 DNA fragments that detect RFLPs in 13 distinct physical regions of the short arm of chromosome 5.
Overhauser J; McMahan J; Wasmuth JJ
Nucleic Acids Res; 1987 Jun; 15(11):4617-27. PubMed ID: 2884625
[TBL] [Abstract][Full Text] [Related]
2. Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes.
Lerman MI; Latif F; Glenn GM; Daniel LN; Brauch H; Hosoe S; Hampsch K; Delisio J; Orcutt ML; McBride OW
Hum Genet; 1991 Apr; 86(6):567-77. PubMed ID: 1673958
[TBL] [Abstract][Full Text] [Related]
3. A fine structure physical map of the short arm of chromosome 5.
Overhauser J; Beaudet AL; Wasmuth JJ
Am J Hum Genet; 1986 Nov; 39(5):562-72. PubMed ID: 2878609
[TBL] [Abstract][Full Text] [Related]
4. Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel.
Gerber MJ; Drabkin HA; Firnhaber C; Miller YE; Scoggin CH; Smith DI
Am J Hum Genet; 1988 Oct; 43(4):442-51. PubMed ID: 2902784
[TBL] [Abstract][Full Text] [Related]
5. Isolation of polymorphic DNA fragments from human chromosome 4.
Gilliam TC; Healey ST; MacDonald ME; Stewart GD; Wasmuth JJ; Tanzi RE; Roy JC; Gusella JF
Nucleic Acids Res; 1987 Feb; 15(4):1445-58. PubMed ID: 2881276
[TBL] [Abstract][Full Text] [Related]
6. Isolation and analysis of DNA markers specific to human chromosome 15.
Tasset DM; Hartz JA; Kao FT
Am J Hum Genet; 1988 Jun; 42(6):854-66. PubMed ID: 2897161
[TBL] [Abstract][Full Text] [Related]
7. Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.
Wieacker P; Davies KE; Cooke HJ; Pearson PL; Williamson R; Bhattacharya S; Zimmer J; Ropers HH
Am J Hum Genet; 1984 Mar; 36(2):265-76. PubMed ID: 6324578
[TBL] [Abstract][Full Text] [Related]
8. Construction of a chromosome 16-enriched phage library and characterization of several DNA segments from 16p.
Harris P; Lalande M; Stroh H; Bruns G; Flint A; Latt SA
Hum Genet; 1987 Oct; 77(2):95-103. PubMed ID: 2888723
[TBL] [Abstract][Full Text] [Related]
9. Parental origin of chromosome 5 deletions in the cri-du-chat syndrome.
Overhauser J; McMahon J; Oberlender S; Carlin ME; Niebuhr E; Wasmuth JJ; Lee-Chen J
Am J Med Genet; 1990 Sep; 37(1):83-6. PubMed ID: 1978567
[TBL] [Abstract][Full Text] [Related]
10. Regional mapping of unique DNA sequences from human chromosome 3 derived from a flow-sorted chromosome library.
Atchison LM; Naylor SL; Freed JJ; Comis RL
Cytogenet Cell Genet; 1988; 48(3):156-9. PubMed ID: 2906850
[TBL] [Abstract][Full Text] [Related]
11. Characterization and regional mapping of new anonymous chromosome 20-specific DNA markers isolated from a flow-sorted DNA library.
Stolz FM; Pfau HP; Reipen G; Schnittger S; Grzeschik KH; Hansmann I
Genomics; 1991 Dec; 11(4):948-55. PubMed ID: 1686021
[TBL] [Abstract][Full Text] [Related]
12. Isolation and analysis of DNA marker revealing restriction fragment length polymorphism from X chromosome specific DNA library.
Sadakane Y
Fukuoka Igaku Zasshi; 1989 Aug; 80(8):404-15. PubMed ID: 2573569
[TBL] [Abstract][Full Text] [Related]
13. Regional assignment of 41 human DNA fragments on chromosome 7 by means of a somatic cell hybrid panel.
Jobs A; Klein-Bölting D; Jandel AS; Driesel A; Olek K; Grzeschik KH
Hum Genet; 1990 Jan; 84(2):147-50. PubMed ID: 1967587
[TBL] [Abstract][Full Text] [Related]
14. Construction of a map of the short arm of human chromosome 6.
Leach R; DeMars R; Hasstedt S; White R
Proc Natl Acad Sci U S A; 1986 Jun; 83(11):3909-13. PubMed ID: 3012539
[TBL] [Abstract][Full Text] [Related]
15. Molecular genetics of human chromosome 4.
Gusella JA; Gilliam TC; MacDonald ME; Cheng SV; Tanzi RE
J Med Genet; 1986 Jun; 23(3):193-9. PubMed ID: 2941587
[TBL] [Abstract][Full Text] [Related]
16. Sixty-five radiation hybrids for the short arm of human chromosome 6: their value as a mapping panel and as a source for rapid isolation of new probes using repeat element-mediated PCR.
Zoghbi HY; McCall AE; LeBorgne-Demarquoy F
Genomics; 1991 Apr; 9(4):713-20. PubMed ID: 1674731
[TBL] [Abstract][Full Text] [Related]
17. The X chromosome shows less genetic variation at restriction sites than the autosomes.
Hofker MH; Skraastad MI; Bergen AA; Wapenaar MC; Bakker E; Millington-Ward A; van Ommen GJ; Pearson PL
Am J Hum Genet; 1986 Oct; 39(4):438-51. PubMed ID: 2876629
[TBL] [Abstract][Full Text] [Related]
18. Isolation and characterization of DNA probes from a flow-sorted human chromosome 8 library that detect restriction fragment length polymorphism (RFLP).
Wood S; Starr TV; Shukin RJ
Am J Hum Genet; 1986 Dec; 39(6):744-50. PubMed ID: 2879441
[TBL] [Abstract][Full Text] [Related]
19. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
Nicholls RD; Knoll JH; Glatt K; Hersh JH; Brewster TD; Graham JM; Wurster-Hill D; Wharton R; Latt SA
Am J Med Genet; 1989 May; 33(1):66-77. PubMed ID: 2568752
[TBL] [Abstract][Full Text] [Related]
20. Isolation and regional localization of 35 unique anonymous DNA markers for human chromosome 22.
Budarf ML; McDermid HE; Sellinger B; Emanuel BS
Genomics; 1991 Aug; 10(4):996-1002. PubMed ID: 1680800
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]