Prenatal diagnosis of fragile X syndrome
- 12 October 1991
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 338 (8772) , 956-958
- https://doi.org/10.1016/0140-6736(91)91831-e
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
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- 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
- FEASIBILITY OF FRAGILE X CHROMOSOME PRENATAL DIAGNOSIS DEMONSTRATEDThe Lancet, 1981
- Fragile Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture MediumScience, 1977