Literature DB >> 2571875

Prenatal detection of major cystic fibrosis mutation.

D J Halley, N H van Damme, W H Deelen, B A Oostra, M G Jahoda, E S Sachs, F J Los, M F Niermeijer.   

Abstract

Entities:  

Mesh:

Year:  1989        PMID: 2571875     DOI: 10.1016/s0140-6736(89)90973-2

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


× No keyword cloud information.
  5 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.  Rapid determination of fetal sex using amniotic fluid cells and the polymerase chain reaction.

Authors:  O Kurauchi; H Yagami; M Kasugai; S Mizutani; Y Tomoda
Journal:  Arch Gynecol Obstet       Date:  1992       Impact factor: 2.344

Review 3.  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

4.  Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype.

Authors:  H J Veeze; D J Halley; J Bijman; J C de Jongste; H R de Jonge; M Sinaasappel
Journal:  J Clin Invest       Date:  1994-02       Impact factor: 14.808

5.  Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Application in the identification of a cystic fibrosis patient with atypical clinical course.

Authors:  W Poller; J P Faber; S Scholz; K Olek; K M Müller
Journal:  Klin Wochenschr       Date:  1991-09-16
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.