# Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/common-chromosomal-fragile-site-fra16d-sequence-identification-of-the-for-gene/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Karin Ried |
| Citations | 273 |
| DOI | 10.1093/hmg/9.11.1651 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | true |
| OA Status | bronze |
| OA URL | https://academic.oup.com/hmg/article-pdf/9/11/1651/9813752/091651.pdf |
| OpenAlex ID | https://openalex.org/W2130679565 |
| PMID | 10861292 |
| Type | article |
| Year | 2000 |

## Paper authors

- [Karin Ried](https://scholariq.org/researchers/karin-ried/)

## Paper primary topic

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Paper topics

- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Chromatin Remodeling and Cancer](https://scholariq.org/topics/chromatin-remodeling-and-cancer/)
- [Signaling Pathways in Disease](https://scholariq.org/topics/signaling-pathways-in-disease/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.