Literature DB >> 8432550

An extended genetic linkage map and an "index" map for human chromosome 17.

P O'Connell1, R Plaetke, N Matsunami, S Odelberg, L Jorde, P Chance, M Leppert, J M Lalouel, R White.   

Abstract

Our previous genetic map for chromosome 17 has been expanded to include 72 loci defined by 90 RFLP markers and four microsatellite markers assayed by the polymerase chain reaction. Forty-one of these loci were ordered with odds greater than 1000:1 against local inversion, and the other 31 were ordered within 95% confidence limits. From the set of 41 unambiguously mapped loci, 14 well-spaced "index markers" can be extracted for efficient genetic studies. The complete map spans 173 cM (136 cM in males and 214 cM in females); average spacing between markers is 4.2 cM.

Entities:  

Mesh：

Substances：

Year:  1993        PMID： 8432550     DOI： 10.1006/geno.1993.1007

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  9 in total

1.  A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels.

Authors:  S C Gerken; H Albertsen; T Elsner; L Ballard; P Holik; E Lawrence; M Moore; X Zhao; R White
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

2.  Two statistical tests for meiotic breakpoint analysis.

Authors:  R Plaetke; G A Schachtel
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

3.  Genetic mapping of the BRCA1 region on chromosome 17q21.

Authors:  H Albertsen; R Plaetke; L Ballard; E Fujimoto; J Connolly; E Lawrence; P Rodriguez; M Robertson; P Bradley; B Milner
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

4.  Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping.

Authors:  L B Jorde; W S Watkins; D Viskochil; P O'Connell; K Ward
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

5.  A common region of deletion on chromosome 17q in both sporadic and familial epithelial ovarian tumors distal to BRCA1.

Authors:  A K Godwin; L Vanderveer; D C Schultz; H T Lynch; D A Altomare; K H Buetow; M Daly; L A Getts; A Masny; N Rosenblum
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

6.  Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.

Authors:  T L Kojis; C Heinzmann; P Flodman; J T Ngo; R S Sparkes; M A Spence; J B Bateman; J R Heckenlively
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

7.  Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families.

Authors:  M Bayés; D Valverde; S Balcells; D Grinberg; L Vilageliu; J Benítez; C Ayuso; M Beneyto; M Baiget; R Gonzàlez-Duarte
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

8.  A radiation hybrid map of the BRCA1 region.

Authors:  P O'Connell; H Albertsen; N Matsunami; T Taylor; J E Hundley; T L Johnson-Pais; B Reus; E Lawrence; L Ballard; R White
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

9.  Deletion mapping on chromosome 17p in medulloblastoma.

Authors:  E Steichen-Gersdorf; M Baumgartner; A Kreczy; H Maier; F M Fink
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.