Improved sizing of fragile X CCG repeats by nested polymerase chain reaction
- 15 July 1994
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 51 (4), 527-534
- https://doi.org/10.1002/ajmg.1320510448
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation.Journal of Medical Genetics, 1992
- Reliable gender screening for human preimplantation embryos, using multiple DNA target-sequencesHuman Reproduction, 1992
- Polymerase chain reaction analysis of fragile X mutationsHuman Genetics, 1992
- Detection of full fragile X mutationThe Lancet, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- 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
- Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X SyndromeScience, 1991
- Rapid cloning of HLA-A,B cDNA by using the polymerase chain reaction: frequency and nature of errors produced in amplification.Proceedings of the National Academy of Sciences of the United States of America, 1990
- Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningHuman Genetics, 1989