GUTHRIE SPOTS FOR DNA-BASED CARRIER TESTING IN CYSTIC FIBROSIS

The Lancet

Volumn 332, Issue 8612, 1988, Pages 693-

  Williams, Carolyn ^a   Weber, Lisa ^a   Williamson, Robert ^a   Hjelm, Magnus ^b  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b HOSPITAL FOR SICK CHILDREN   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CYSTIC FIBROSIS; GUTHRIE TEST; HUMAN; LETTER; PRIORITY JOURNAL;

CYSTIC FIBROSIS; DNA; GENETIC SCREENING; HUMAN; MALE; PEDIGREE; SUPPORT, NON-U.S. GOV'T;

EID: 0023684670     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(88)90512-0     Document Type: Letter

References (7)

1. Diagnosis of genetic disease using recombinant DNA
2. An improved method for pre-natal diagnosis of genetic diseases by analysis of amplified DNA sequences
3. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia
4. Same-day first-trimester antenatal diagnosis for cystic fibrosis by gene amplification
5. A simple non-invasive method to obtain DNA for gene analysis
6. A candidate for the cystic fibrosis locus isolated by selection of methylation-free islands
7. First-trimester prenatal diagnosis of cystic fibrosis with linked DNA probes