Borderline repeat expansion in Huntington's disease

The Lancet

Volumn 342, Issue 8885, 1993, Pages 1491-1492

  de Rooij, K E ^a,b   de Koning Gans, P A M ^a,b   Losekoot, M ^a,b   Bakker, E ^a,b   den Dunnen, J T ^a,b   Vegter van der Vlis, M ^a,b   Roos, R A C ^a,b   van Ommen, G J B ^a,b  

^a Department of Human Genetics   (Netherlands)

^b LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; BORDERLINE STATE; GENETIC COUNSELING; HUMAN; HUNTINGTON CHOREA; LETTER; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT;

ALLELES; BASE SEQUENCE; DNA PRIMERS; FEMALE; FETAL DISEASES; GENETIC COUNSELING; HUMAN; HUNTINGTON DISEASE; MALE; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; PREDICTIVE VALUE OF TESTS; PREGNANCY; PRENATAL DIAGNOSIS; PROTEINS; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0027138068     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/0140-6736(93)92974-X     Document Type: Article

References (6)

1. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromsomes
2. n repeat in sporadic Huntington's disease
3. Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effect
4. A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes