Literature DB >> 5928007

Diagnosis of heterozygosity for cystic fibrosis by discriminatory analysis of sweat chloride distribution.

A Sproul, N Huang.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1966        PMID: 5928007     DOI: 10.1016/s0022-3476(66)80122-1

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  5 in total

1.  The relevance of sweat testing for the diagnosis of cystic fibrosis in the genomic era.

Authors:  Avantika Mishra; Ronda Greaves; John Massie
Journal:  Clin Biochem Rev       Date:  2005-11

Review 2.  Screening, early neonatal diagnosis and prenatal diagnosis.

Authors:  J A Kuzemko
Journal:  J R Soc Med       Date:  1986       Impact factor: 5.344

3.  Cystic fibrosis: present status and future prospects in detection of patients and carriers.

Authors:  G Forstner; D N Crozier; J M Sturgess
Journal:  Can Med Assoc J       Date:  1975-09-20       Impact factor: 8.262

Review 4.  The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive Therapy.

Authors:  Philip M Farrell; Michael J Rock; Mei W Baker
Journal:  Genes (Basel)       Date:  2020-04-08       Impact factor: 4.096

5.  Cystic fibrosis of the pancreas. A study in cell culture.

Authors:  B S Danes; A G Bearn
Journal:  J Exp Med       Date:  1969-04-01       Impact factor: 14.307

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.