# Fragile X syndrome and deletions in FMR1: New case and review of the literature

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/fragile-x-syndrome-and-deletions-in-fmr1-new-case-and-review-of-the-literature/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Lyn S. Hammond,Michelle M. Macias,Jack Tarleton,G. Shashidhar Pai |
| Citations | 145 |
| DOI | 10.1002/(sici)1096-8628(19971112)72:4<430::aid-ajmg11>3.0.co;2-s |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W1989326324 |
| PMID | 9375726 |
| Type | article |
| Year | 1997 |

## Paper authors

- [Michelle M. Macias](https://scholariq.org/researchers/michelle-m-macias/)

## 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/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Ubiquitin and proteasome pathways](https://scholariq.org/topics/ubiquitin-and-proteasome-pathways/)

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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.