Fragile-X syndrome in east Finland: Molecular approach to genetic and prenatal diagnosis
- 15 July 1994
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 51 (4) , 463-465
- https://doi.org/10.1002/ajmg.1320510433
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Fragile X Genotype Characterized by an Unstable Region of DNAScience, 1991
- Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X SyndromeScience, 1991
- Preventive Screening for the Fragile X SyndromeNew England Journal of Medicine, 1986