Last Posted: Jun-07-2019 1PM
Last Posted: Jun 05, 2019
- Bespoke Babies: Genome Editing in Cystic Fibrosis Embryos.
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Krishnananthan Thanuja et al. Paediatric respiratory reviews 2019 Mar - Interventions for promoting participation in shared decision-making for children and adolescents with cystic fibrosis.
Malone Helen et al. The Cochrane database of systematic reviews 2019 May 5CD012578 - Gene and Base Editing as a Therapeutic Option for Cystic Fibrosis-Learning from Other Diseases.
Mention Karen et al. Genes 2019 May 10(5) - Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka.
Indika Neluwa Liyanage Ruwan et al. BMC medical genetics 2019 May 20(1) 89 - Cystic Fibrosis Patients Turn to Experimental Phage Therapy
A Ellin, NY Times, May 17, 2019 - International approaches for delivery of positive newborn bloodspot screening results for CF.
Chudleigh J et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2019 Apr - Sequencing as a first-line methodology for cystic fibrosis carrier screening.
Beauchamp Kyle A et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Apr - A Review on the Use of Cystic Fibrosis Transmembrane Conductance Regulator Gene Modulators in Pediatric Patients.
Bitonti Michael et al. Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & Practitioners 33(3) 356-364 - Inconclusive diagnosis after a positive newborn bloodspot screening result for cystic fibrosis; clarification of the harmonised international definition.
Southern K W et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2019 Apr
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