Genetic screening for cystic fibrosis

Obstetrics and Gynecology Clinics of North America

Volumn 29, Issue 2, 2002, Pages 329-340

  Gregg, Anthony R ^a   Simpson, Joe Leigh ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CYSTIC FIBROSIS; ETHNOLOGY; GENETIC SCREENING; GENOTYPE; HIGH RISK POPULATION; HUMAN; LUNG FUNCTION; MUTATION; PHENOTYPE; PRIORITY JOURNAL; REVIEW; FEMALE; GENETIC COUNSELING; GENETICS; HETEROZYGOTE; METHODOLOGY; MOLECULAR BIOLOGY; NUCLEOTIDE SEQUENCE; PATIENT EDUCATION; PREGNANCY; PRENATAL DIAGNOSIS; SENSITIVITY AND SPECIFICITY;

CYSTIC FIBROSIS; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; HETEROZYGOTE; HUMAN; MOLECULAR BIOLOGY; MUTATION; PATIENT EDUCATION; PREGNANCY; PRENATAL DIAGNOSIS; SENSITIVITY AND SPECIFICITY; HUMANS;

EID: 0035989793     PISSN: 08898545     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0889-8545(02)00005-0     Document Type: Review

References (17)

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2. Some organic digestive disturbances in early life
3. Celiac syndrome. V. Genetics of cystic fibrosis of the pancreas with a consideration of etiology
4. Identification of the cystic fibrosis gene: Genetic analysis
5. Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA
6. Identification of the cystic fibrosis gene: Chromosome walking and jumping
7. Cystic fibrosis
8. Cystic fibrosis
9. The clinical significance of fetal echogenic bowel
10. Glucose intolerance in cystic fibrosis
11. Serum alkaline phosphatase in cystic fibrosis: Interpretation of elevated values based on electrophoretic isoenzyme analyses
12. The cost-effectiveness of prenatal carrier screening for cystic fibrosis
13. Low blood pressure in young adults with cystic fibrosis: An effect of chronic salt loss in sweat?
14. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations
15. Laboratory standards and guidelines for population-based cystic fibrosis carrier screening