Ordering of 66 STSs along the entire short arm of human chromosome 17 and chromosome assignment of a transcribed sequence (FMR1L2) homologous to FMR1

Cytogenetics and Cell Genetics

Volumn 73, Issue 3, 1996, Pages 240-243

  Wilgenbus, K K ^a   Coy, J F ^a   Mincheva, A ^a   Nicolai, H ^b   Solomon, E ^b   Lichter, P ^a   Poustka, A ^a  

^a GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^b Imperial Cancer Research Fund   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CHROMOSOME 17P; CHROMOSOME BREAKAGE; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; DNA TRANSCRIPTION; GENE ASSIGNMENT; GENE LOCATION; GENE MAPPING; GENETIC LINKAGE; HUMAN; HUMAN CELL; HYBRID CELL; MOUSE; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; SEQUENCE TAGGED SITE; YEAST ARTIFICIAL CHROMOSOME;

ANIMALS; BASE SEQUENCE; CELL LINE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 17; CRICETINAE; DNA PRIMERS; FRAGILE X MENTAL RETARDATION PROTEIN; HUMANS; MICE; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; RNA-BINDING PROTEINS; SEQUENCE TAGGED SITES; TRANSCRIPTION, GENETIC;

ANIMALIA;

EID: 0030056672     PISSN: 03010171     EISSN: 1424859X     Source Type: Journal    
DOI: 10.1159/000134347     Document Type: Article

References (16)

1. Black D, Nicolai H, Borrow J, Solomon E: A somatic cell hybrid map of the long arm of human chromosome 17, containing the familial breast cancer locus (BRCA1). Am J hum Genet 52: 702-710 (1993).
2. Camuzat A, Dollfus H. Rozet J-M, Gerber S., Bonneau D, Bonnemaison M. Briard M-L. Dufier J-L. Ghazi I, Leowski C, Weissenbach J, Frezal J, Munnich A. Kaplan J: A gene for Leber's amaurosis maps to chromosome 17p. Hum mol Genet 4:1447-1452 (1995).
3. Cox D, Burmeister M, Price ER. Kim S. Myers RS: Radiation hybrid mapping: A somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. Science 250:245-250 (1990).
4. Coy JF, Sedlacek Z, Baechner D. Hameister H, Joos S. Lichter P. Delius H, Poustka A: Highly conserved 3'UTR and expression pattern of FXR1 points to a divergent gene regulation of FXRI and FMR1. Hum mol Genet 4:2209-2218 (1995).
5. Friedman TB. Liang YL. Weber JL, Hinnant JT. Barber TD, Winata S, Arhya IN, Asher JH Jr: A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17. Nature Genet 6:86-91 (1995).
6. Gerken SC. Albertsen H, Eisner T. Ballard L. Holik L, Lawrence E. Moore M, Zhao Z, White R: A strategy for constructing high-resolution genetic maps of the human genome: A genetic map of chromosome 17p. ordered with meiotic breakpoint-mapping panels. Am J hum Genet 56:484-499 (1995).
7. Kelsell DP. Rooke L, Warne D. Bouzyk M. Cullin L, Cox S, West L. Povey S. Spurr NK: Development of a panel of monochromosomal somatic cell hybrids for rapid gene mapping. Ann hum Genet 59:233-241 (1995).
8. Lichter P. Tang CC, Call K. Hermanson G. Evans GA, Housman D. Ward DC: High resolution mapping of human chromosome 11 by in-situ hybridization with cosmid clones. Science 247:64-69 (1990).
9. Makos-Wales M, Biel MA, Deiry WE, Nelkin BD, Issa J-P, Cavenec WK, Kuerbitz SJ, Baylin SB: p53 activates expression of HIC-I. a new candidate tumour suppressor gene on 17pl 3.3. Nature Medicine 1:570-577 (1995).
10. Morton NE: Parameters of the human genome. Proc natl Acad Sci, USA 88:7474-7476 (1991).
11. Raeymaekers P. van Zand K. Jun L. Höglund M. Cassiman JJ. van den Berghe H. Marynen P: A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12. Genomics 29:170-178 (1995).
12. Smith ACM, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, Reiss J, Lahr M, Allen L, Magenis E: Interstitial deletion of (I7)(pl 1.2 pi 1.2): Report of six additional patients with a new chromosome deletion syndrome. Am J med Genet 24:393-414(1986)
13. Takita K, Sato T, Miyagi M, Watanani M, Akiyama F, Sakamoto G, Kasumi F, Abe R, Nakamura Y: Correlation of loss of alleles on the short arm of chromosome 11 and 17 with metastasis of primary breast cancer to lymph nodes, Cancer Res 52: 3914-3917 (1992).
14. The Cystinosis Collaborative Research Group: Linkage of the gene for cystinosis to markers on the short arm of chromosome 17. Nature Genet 10:246-248 (1995).
15. The Utah marker development group: A collection of ordered tetranucleotidc-rcpcat markers from the human genome. Am J hum Genet 57:619-628 (1995).
16. Wilgenbus K, Mincheva A, Korn B, Lichter P, Poustka A: IRS-long range PCR: A simple method for amplification of human genomic DNA from complex sources. Meth mol Cell Biol 5:214-221 (1995).