Incidence, Etiology and Prognosis of First-Time Acute Pancreatitis in Young Patients: A Population-Based Cohort Study.

Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European population.

Original research: parents and children with cystic fibrosis.

A high frequency of the Cystic Fibrosis 2184insA mutation in Western Ukraine: Genotype-phenotype correlations, relevance for newborn screening and genetic testing.

PGD for all cystic fibrosis carrier couples: novel strategy for preventive medicine and cost analysis.

Declining prevalence of cystic fibrosis since the introduction of newborn screening.

Health insurance coverage of genetic services in Illinois.

Uptake of carrier testing in families after cystic fibrosis diagnosis through newborn screening.

Genetic factors in chronic pancreatitis; implications for diagnosis, management and prognosis.

Genetic, epidemiological, and clinical aspects of hereditary pancreatitis: a population-based cohort study in Denmark.

Carrier screening for cystic fibrosis.

Ashkenazi Jewish screening in the twenty-first century.

Impact of gene patents and licensing practices on access to genetic testing and carrier screening for Tay-Sachs and Canavan disease.

Impact of gene patents and licensing practices on access to genetic testing for cystic fibrosis.

Gene patents and licensing: case studies prepared for the Secretary's Advisory Committee on Genetics, Health, and Society.

Genetic counselling issues in cystic fibrosis.

Genetic testing in pancreatitis.

Declining prevalence of cystic fibrosis since the introduction of newborn screening.

Diagnosis of adult hereditary pulmonary disease and the role of genetic testing: it is all about the genes.

Benchmarks for cystic fibrosis carrier screening: a European consensus document.

Cystic fibrosis newborn screening.

Outcomes of a cystic fibrosis carrier testing clinic for couples.

Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation.

Long-term evaluation of genetic counseling following false-positive newborn screen for cystic fibrosis.

Multifunctional nanocomplexes for gene transfer and gene therapy.