Frequency of four cystic fibrosis mutations in a Swedish population-Reference-Cited by-同舟云学术

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Frequency of four cystic fibrosis mutations in a Swedish population

Published:1993-06 Issue:6-7 Volume:82 Page:609-609
ISSN:0803-5253
Container-title:Acta Paediatrica
language:en
Short-container-title:Acta Paediatrica

Author:

Dahl N,Grandell U,Martinsson T,Allen M,Johansson L,Stolpe L,Gyllensten U,Hjelte L,Kollberg H,Strandvik B,Wahlstrom J,Anvret M

Publisher

Wiley

Subject

General Medicine,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1993.tb12769.x/fullpdf

Reference6 articles.

1. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA

2. Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping

3. Identification of the Cystic Fibrosis Gene: Genetic Analysis

4. Frequency of the F508 deletion in the CFTR gene in Turkish cystic fibrosis patients

5. Severity of cystic fibrosis in patients homozygous and heterozygous for ΔF508 mutation

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Potential role for the common cystic fibrosis ΔF508 mutation in Crohnʼs disease;Inflammatory Bowel Diseases;2007-05

2. Maternal and fetal morbidity in pregnancies of Norwegian and Swedish women with cystic fibrosis;Acta Obstetricia et Gynecologica Scandinavica;2002-08

3. Three common CFTR mutations should be included in a neonatal screening programme for cystic fibrosis in Sweden;Clinical Genetics;1999-10

4. Female patients with cystic fibrosis suffer from reproductive endocrinological disorders despite good clinical status;Human Reproduction;1998-08-01

5. Neonatal screening for the cystic fibrosis main mutation ΔF508 in Estonia;Journal of Medical Screening;1998-03-01

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