Literature DB >> 1677924

Choroideremia: linkage analysis with physically mapped close DNA-markers.

E M Sankila1, P Sistonen, F Cremers, A de la Chapelle.   

Abstract

We report linkage studies in 18 choroideremia (TCD) families using four closely linked polymorphic markers. Probe pZ11, which is known to be deleted in several unrelated patients with TCD, showed no recombinations (zeta max 15.63 at theta = 0.00). In contrast, one recombination was observed with DXS367, which is also physically very close to TCD. Loci DXS95 and DXYS69 each showed more than one recombination with TCD. Moreover, these analyses revealed a double crossover between TCD and DXYS1, changing the previously reported very close linkage to a recombination fraction of 0.04 with a lod score of 9.93. Multipoint linkage analysis placed TCD proximal to DXS95-DXYS69 and very close to DXS367-pZ11 with almost identical multipoint lod score maxima either proximal to DXS367 (zeta max = 23.43) or proximal to pZ11 (zeta max = 23.36). These results provide a refined linkage map around TCD and will also be useful in DNA diagnostics of the disease.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1677924     DOI: 10.1007/bf00200918

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  37 in total

1.  Individual-specific 'fingerprints' of human DNA.

Authors:  A J Jeffreys; V Wilson; S L Thein
Journal:  Nature       Date:  1985 Jul 4-10       Impact factor: 49.962

Review 2.  Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms.

Authors:  K K Kidd; A M Bowcock; J Schmidtke; R K Track; F Ricciuti; G Hutchings; A Bale; P Pearson; H F Willard; J Gelernter
Journal:  Cytogenet Cell Genet       Date:  1989

3.  Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).

Authors:  Y Nakamura; S Gillilan; P O'Connell; M Leppert; G M Lathrop; J M Lalouel; R White
Journal:  Nucleic Acids Res       Date:  1987-12-10       Impact factor: 16.971

4.  The genetic linkage map of the human X chromosome.

Authors:  D Drayna; R White
Journal:  Science       Date:  1985-11-15       Impact factor: 47.728

5.  Choroideremia. A clinical and genetic study of 84 Finnish patients and 126 female carriers.

Authors:  J Kärnä
Journal:  Acta Ophthalmol Suppl       Date:  1986

6.  DXS165 detects a translocation breakpoint in a woman with choroideremia and a de novo X; 13 translocation.

Authors:  D E Merry; J G Lesko; V Siu; W F Flintoff; F Collins; R A Lewis; R L Nussbaum
Journal:  Genomics       Date:  1990-04       Impact factor: 5.736

7.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

8.  Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.

Authors:  I M MacDonald; R M Sandre; P Wong; A G Hunter; M P Tenniswood
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

9.  Choroideremia: further evidence for assignment of the locus to Xq13-Xq21.

Authors:  M Schwartz; T Rosenberg; E Niebuhr; C Lundsteen; H Sardemann; O Andersen; H M Yang; L U Lamm
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

10.  Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Authors:  F P Cremers; D J van de Pol; B Wieringa; F S Collins; E M Sankila; V M Siu; W F Flintoff; F Brunsmann; L A Blonden; H H Ropers
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

View more
  3 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

2.  Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypes.

Authors:  T I Elsner; H Albertsen; S C Gerken; P Cartwright; R White
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

Review 3.  Disease gene mapping in isolated human populations: the example of Finland.

Authors:  A de la Chapelle
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.