# The Coffin-Lowry syndrome: An inherited faciodigital mental retardation syndrome

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/the-coffin-lowry-syndrome-an-inherited-faciodigital-mental-retardation-syndrome/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Samia A. Temtamy,Jordan Miller,Irene Hussels-Maumenee |
| Citations | 85 |
| DOI | 10.1016/s0022-3476(75)80357-x |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2035782355 |
| PMID | 1133653 |
| Type | article |
| Year | 1975 |

## Paper authors

- [Jordan Miller](https://scholariq.org/researchers/jordan-miller/)

## Paper journal

- [The Journal of Pediatrics](https://scholariq.org/journals/the-journal-of-pediatrics/)

## 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/)
- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [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.