Literature DB >> 2323777

In situ hybridization studies using a molecular probe that maps to Xq27-Zq28.

A M Duncan1, C Morgan.   

Abstract

The locus DXS98, which is recognized by the sequence p4D-8, is closely linked to the FRAXA locus. In this study we present data that confirm the existing mapping data, sublocalizing this sequence to the Xq27 region immediately proximal to the fragile site at Xq27.3.

Entities:  

Mesh：

Substances：

Year:  1990        PMID： 2323777     DOI： 10.1007/bf00195817

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


  13 in total

Review 1.  Fragile X syndrome: a unique mutation in man.

Authors:  R L Nussbaum; D H Ledbetter
Journal:  Annu Rev Genet       Date:  1986       Impact factor: 16.830

2.  Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

Authors:  M Patterson; S Kenwrick; S Thibodeau; K Faulk; M G Mattei; J F Mattei; K E Davies
Journal:  Nucleic Acids Res       Date:  1987-03-25       Impact factor: 16.971

3.  RFLP for linkage analysis of fragile X syndrome.

Authors:  W T Brown; Y Wu; A C Gross; C B Chan; C S Dobkin; E C Jenkins
Journal:  Lancet       Date:  1987-01-31       Impact factor: 79.321

4.  Deleted X chromosomes in patients with the fragile X syndrome.

Authors:  M Fitchett; M Seabright
Journal:  J Med Genet       Date:  1984-10       Impact factor: 6.318

5.  The fragile X: a scanning electron microscope study.

Authors:  C J Harrison; E M Jack; T D Allen; R Harris
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

6.  Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations.

Authors:  M S Krawczun; E C Jenkins; W T Brown
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  Localization of single copy DNA sequences of G-banded human chromosomes by in situ hybridization.

Authors:  M E Harper; G F Saunders
Journal:  Chromosoma       Date:  1981       Impact factor: 4.316

8.  Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

Authors:  M G Mattei; M A Baeteman; R Heilig; I Oberlé; K Davies; J L Mandel; J F Mattei
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.

Authors:  P Szabo; M Purrello; M Rocchi; N Archidiacono; B Alhadeff; G Filippi; D Toniolo; G Martini; L Luzzatto; M Siniscalco
Journal:  Proc Natl Acad Sci U S A       Date:  1984-12       Impact factor: 11.205

10.  The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.

Authors:  M Purrello; B Alhadeff; D Esposito; P Szabo; M Rocchi; M Truett; F Masiarz; M Siniscalco
Journal:  EMBO J       Date:  1985-03       Impact factor: 11.598
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.