Literature DB >> 3481306

Deletion of the DXS165 locus in patients with classical choroideremia.

F P Cremers1, F Brunsmann, T J van de Pol, I H Pawlowitzki, K Paulsen, B Wieringa, H H Ropers.   

Abstract

Using various probes from the Xq21 region which is known to carry the choroideremia (tapetochoroideal dystrophy, TCD) locus, we have screened the DNAs from eight unrelated male choroidermia patients for microdeletions. In two of these patients, but not in any of 45 males tested as controls, lack of hybridization signals with probe plbD5 suggested a deletion encompassing the DXS165 locus and (part of) the TCD gene. Absence of additional clinical features in these patients and the fact that two closely linked, and probably flanking, TCD markers (DXYS1 and DXS72) are not deleted may indicate that the physical distance between the DXS165 locus and the TCD gene is small.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3481306     DOI: 10.1111/j.1399-0004.1987.tb03166.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  12 in total

1.  Linkage studies and deletion screening in choroideremia.

Authors:  A F Wright; R L Nussbaum; S S Bhattacharya; M Jay; J G Lesko; H J Evans; B Jay
Journal:  J Med Genet       Date:  1990-08       Impact factor: 6.318

2.  Derivation of clones from the choroideremia locus by preparative field inversion gel electrophoresis.

Authors:  T J van de Pol; F P Cremers; R M Brohet; B Wieringa; H H Ropers
Journal:  Nucleic Acids Res       Date:  1990-02-25       Impact factor: 16.971

3.  The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Authors:  H G Brunner; A van Bennekom; E M Lambermon; T L Oei; W R Cremers; B Wieringa; H H Ropers
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

4.  Haplotype and multipoint linkage analysis in Finnish choroideremia families.

Authors:  E M Sankila; T Lehner; A W Eriksson; H Forsius; J Kärnä; D Page; J Ott; A de la Chapelle
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

5.  Multimodal assessment of choroideremia patients defines pre-treatment characteristics.

Authors:  Immanuel P Seitz; Ahmad Zhour; Susanne Kohl; Pablo Llavona; Tobias Peter; Barbara Wilhelm; Eberhart Zrenner; Marius Ueffing; Karl Ulrich Bartz-Schmidt; M Dominik Fischer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-03-07       Impact factor: 3.117

6.  Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.

Authors:  F P Cremers; E M Sankila; F Brunsmann; M Jay; B Jay; A Wright; A J Pinckers; M Schwartz; D J van de Pol; B Wieringa
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

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

Authors:  E M Sankila; P Sistonen; F Cremers; A de la Chapelle
Journal:  Hum Genet       Date:  1991-07       Impact factor: 4.132

8.  Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

Authors:  F P Cremers; T J van de Pol; B Wieringa; M H Hofker; P L Pearson; R A Pfeiffer; M Mikkelsen; A Tabor; H H Ropers
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

9.  Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.

Authors:  D E Merry; J G Lesko; D M Sosnoski; R A Lewis; M Lubinsky; B Trask; G van den Engh; F S Collins; R L Nussbaum
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

10.  Cloning of the breakpoints of a deletion associated with choroidermia.

Authors:  F P Cremers; F Brunsmann; W Berger; E P van Kerkhoff; T J van de Pol; B Wieringa; I H Pawlowitzki; H H Ropers
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.