Fragile X prenatal analyses show full mutation females at high risk for mosaic Turner syndrome: Fragile X leads to chromosome loss
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference22 articles.
1. FMR1 and the fragile X syndrome: Human genome epidemiology review;Crawford;Genet Med,2001
2. Chromosome fragile sites;Durkin;Annu Rev Genet,2007
3. Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island;Heitz;Science,1991
4. The distribution of chromosomal genotypes associated with Turner's syndrome: Livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism;Hook;Hum Genet,1983
5. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n;Kremer;Science,1991
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1. The fragile X locus is prone to spontaneous DNA damage that is preferentially repaired by nonhomologous end-joining to preserve genome integrity;iScience;2024-02
2. Phenotypic variability to medication management: an update on fragile X syndrome;Human Genomics;2023-07-07
3. Fragile sites, chromosomal lesions, tandem repeats, and disease;Frontiers in Genetics;2022-11-17
4. Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosome;BMJ Case Reports;2022-07
5. Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis;Genes;2021-11-27
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