Molecular genetic advances in fragile Xsyndrome
- 28 February 1993
- journal article
- review article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 122 (2) , 169-185
- https://doi.org/10.1016/s0022-3476(06)80110-1
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Molecular heterogeneity of the fragile X syndromeNucleic Acids Research, 1991
- Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) nScience, 1991
- 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
- Population incidence and segregation ratios in the Martin‐Bell syndromeAmerican Journal of Medical Genetics, 1986
- Fragile Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture MediumScience, 1977
- Familial X-linked mental retardation with an X chromosome abnormality.Journal of Medical Genetics, 1977
- Constitutional chromosomal breakageHuman Genetics, 1976
- A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGEJournal of Neurology, Neurosurgery & Psychiatry, 1943