Literature DB >> 2564190

Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplification.

H Northrup1, C Rosenbloom, W E O'Brien, A L Beaudet.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1989        PMID： 2564190      PMCID： PMC331860          DOI： 10.1093/nar/17.4.1784

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


× No keyword cloud information.
  7 in total

1.  Gradient of distribution in Europe of the major CF mutation and of its associated haplotype. European Working Group on CF Genetics (EWGCFG).

Authors: 
Journal:  Hum Genet       Date:  1990-09       Impact factor: 4.132

2.  The Kell blood group locus is close to the cystic fibrosis locus on chromosome 7.

Authors:  K R Purohit; J L Weber; L J Ward; B J Keats
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

3.  Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.

Authors:  J Reiss; D N Cooper; J Bal; R Slomski; G R Cutting; M Krawczak
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132

4.  Approaches to localizing disease genes as applied to cystic fibrosis.

Authors:  M Dean; M L Drumm; C Stewart; B Gerrard; A Perry; N Hidaka; J L Cole; F S Collins; M C Iannuzzi
Journal:  Nucleic Acids Res       Date:  1990-01-25       Impact factor: 16.971

Review 5.  Application of the polymerase chain reaction to the diagnosis of human genetic disease.

Authors:  J Reiss; D N Cooper
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

Review 6.  The cystic fibrosis defect approached from different angles--new perspectives on the gene, the chloride channel, diagnosis and therapy.

Authors:  D J Halley; J Bijman; H R de Jonge; M Sinaasappel; H J Neijens; M F Niermeijer
Journal:  Eur J Pediatr       Date:  1990-07       Impact factor: 3.183

7.  Exclusion of two candidate pigment loci, c and b, part of chromosome 11p, and 33 random polymorphic markers as the locus for tyrosinase-positive oculocutaneous albinism.

Authors:  M A Colman; G Stevens; M Ramsay; B Kwon; T Jenkins
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.