Population Based Prenatal Screening for the Fragile X Syndrome
- 1 January 1994
- journal article
- Published by SAGE Publications in Journal of Medical Screening
- Vol. 1 (1) , 65-72
- https://doi.org/10.1177/096914139400100112
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- The fragile X SyndromePublished by Elsevier ,1992
- Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental RetardationNew England Journal of Medicine, 1991
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 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
- Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell AnemiaScience, 1985
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984
- Fragile Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture MediumScience, 1977