Identification of the Cystic Fibrosis Gene : Chromosome Walking and Jumping Author ( s ) :
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Summary
This review concludes with a call for further research into the determinants of infectious disease and its role in the immune system.
- Published
- 2008-01-01
- Cited by
- 2,029
- References
- 17
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:6351189
References
Cited by
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- Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA.
- Complementation of null CF mice with a human CFTR YAC transgene
- Missense mutation R1066C in the second transmembrane domain of CFTR causes a severe cystic fibrosis phenotype: Study of 19 heterozygous and 2 homozygous patients
- Inheritance and pathogenicity of myotonic dystrophy.
- Pseudomonas aeruginosa Infections in Patients with Cystic Fibrosis
- Molecular-biology approaches to genetic defects of the mammalian nervous system.
- CLINICAL, ANDROLOGICAL AND GENETIC CHARACTERISTICS OF PATIENTS WITH CONGENITAL BILATERAL ABSENCE OF VAS DEFERENS (CBAVD)
- Cystic fibrosis: a review of epidemiology and pathobiology.
- Pseudomonas aeruginosa biofilms: mechanisms of immune evasion.
- Therapeutic Efficacy and Safety of Amitriptyline in Patients with Cystic Fibrosis
- Pitfalls in the Immunohistochemical Localization of the Cystic Fibrosis Transmembrane Conductance Regulator in Paraffin Embedded Sweat Glands
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