Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males
- 31 October 1995
- journal article
- clinical trial
- Published by Elsevier BV in Brain & Development
- Vol. 17 (5), 317-321
- https://doi.org/10.1016/0387-7604(95)00031-6
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Dynamic mutations: A new class of mutations causing human diseaseCell, 1992
- Triplet repeat mutations in human diseaseScience, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental RetardationThe New England Journal of Medicine, 1991
- Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) nScience, 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
- Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndromeCell, 1991
- Preventive Screening for the Fragile X SyndromeThe New England Journal of Medicine, 1986
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985