Literature DB >> 2898671

Same-day, first-trimester antenatal diagnosis for cystic fibrosis by gene amplification.

C Williams, R Williamson, C Coutelle, F Loeffler, J Smith, A Ivinson.   

Abstract

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Year:  1988        PMID： 2898671     DOI： 10.1016/s0140-6736(88)90031-1

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  12 in total

1.  A point mutation changes the polymorphisms pattern in a cystic fibrosis carrier family.

Authors:  E Fernández; A Santón; J Benitez
Journal:  Hum Genet       Date:  1992-06       Impact factor: 4.132

2.  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

3.  Molecular genetics in the National Health Service in Britain.

Authors:  R Harris; R Elles; D Craufurd; A Dodge; A Ivinson; K Hodgkinson; R Mountford; M Schwartz; T Strachan; A Read
Journal:  J Med Genet       Date:  1989-04       Impact factor: 6.318

Review 4.  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

5.  Risks of fetal cystic fibrosis based on linkage disequilibrium data.

Authors:  S Holloway; D J Brock
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

6.  Preimplantation diagnosis with the polymerase chain reaction.

Authors:  A P Read; D Donnai
Journal:  BMJ       Date:  1989-07-01

Review 7.  The polymerase chain reaction: an improved method for the analysis of nucleic acids.

Authors:  H P Vosberg
Journal:  Hum Genet       Date:  1989-08       Impact factor: 4.132

8.  Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS).

Authors:  C R Newton; A Graham; L E Heptinstall; S J Powell; C Summers; N Kalsheker; J C Smith; A F Markham
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

Review 9.  Prenatal diagnosis of common genetic disorders.

Authors:  M D Crawfurd
Journal:  BMJ       Date:  1988 Aug 20-27

10.  Exclusion of COL1A1, COL1A2, and COL3A1 genes as candidate genes for Ehlers-Danlos syndrome type I in one large family.

Authors:  B P Sokolov; A N Prytkov; G Tromp; R G Knowlton; D J Prockop
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132
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