Literature DB >> 7927350

A PvuII polymorphism near exon 2 of the dystrophin gene.

G S Cross1, J T Donnelly, A L Sharif.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1994        PMID： 7927350     DOI： 10.1007/bf00201615

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


× No keyword cloud information.
  5 in total

1.  Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach.

Authors:  A J Coffey; R G Roberts; E D Green; C G Cole; R Butler; R Anand; F Giannelli; D R Bentley
Journal:  Genomics       Date:  1992-03       Impact factor: 5.736

2.  Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Authors:  J T Den Dunnen; P M Grootscholten; E Bakker; L A Blonden; H B Ginjaar; M C Wapenaar; H M van Paassen; C van Broeckhoven; P L Pearson; G J van Ommen
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

3.  Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.

Authors:  A H Beggs; M Koenig; F M Boyce; L M Kunkel
Journal:  Hum Genet       Date:  1990-11       Impact factor: 4.132

4.  Two hot spots of recombination in the DMD gene correlate with the deletion prone regions.

Authors:  C Oudet; A Hanauer; P Clemens; T Caskey; J L Mandel
Journal:  Hum Mol Genet       Date:  1992-11       Impact factor: 6.150

5.  Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.

Authors:  T J Smith; S M Forrest; G S Cross; K E Davies
Journal:  Nucleic Acids Res       Date:  1987-12-10       Impact factor: 16.971
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.