A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome

Hum Genet. 1988 Oct;80(2):193. doi: 10.1007/BF00702869.

Authors

A M Rekilä¹, M L Väisänen, M Kähkönen, J Leisti, R Winqvist

Affiliation

¹ Department of Clinical Genetics, Oulu University Central Hospital, Finland.

PMID: 2902001
DOI: 10.1007/BF00702869

Abstract

The authors report on a new RFLP at DXS105 suitable for carrier detection of fragile X syndrome.

MeSH terms

Deoxyribonucleases, Type II Site-Specific*
Female
Fragile X Syndrome / genetics*
Genetic Carrier Screening*
Genetic Markers*
Humans
Male
Pedigree
Polymorphism, Genetic*
Polymorphism, Restriction Fragment Length*
Sex Chromosome Aberrations / genetics*

Substances

Genetic Markers
AGGCCT-specific type II deoxyribonucleases
Deoxyribonucleases, Type II Site-Specific