Molecular genetics of fragile X: a cytogenetics viewpoint. Report of the Fifth International Symposium on X Linked Mental Retardation, Strasbourg, France, 12 to 16 August 1991 (organiser Dr J-L Mandel).
Open Access
- 1 December 1991
- journal article
- review article
- Published by BMJ in Journal of Medical Genetics
- Vol. 28 (12) , 814-817
- https://doi.org/10.1136/jmg.28.12.814
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Genotype prediction in the fragile X syndrome.Journal of Medical Genetics, 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
- Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndromeCell, 1991
- Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresisNature, 1991