# Further delineation of the oculoauricular syndrome phenotype: A new family with a novel truncating HMX1 mutation

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/further-delineation-of-the-oculoauricular-syndrome-phenotype-a-new-family-with-a/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Ghada M. H. Abdel‐Salam,Mohamed S. Abdel‐Hamid,Mennat Mehrez,Ahmad M. Kamal,Mohamed B. Taher,Hanan H. Afifi |
| Citations | 10 |
| DOI | 10.1080/13816810.2017.1401089 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2768629460 |
| PMID | 29140751 |
| Type | article |
| Year | 2017 |

## Paper authors

- [Mennat Mehrez](https://scholariq.org/researchers/mennat-mehrez/)

## Paper primary topic

- [Ocular Disorders and Treatments](https://scholariq.org/topics/ocular-disorders-and-treatments/)

## Paper topics

- [Ocular Disorders and Treatments](https://scholariq.org/topics/ocular-disorders-and-treatments/)
- [Corneal Surgery and Treatments](https://scholariq.org/topics/corneal-surgery-and-treatments/)
- [Ocular Surface and Contact Lens](https://scholariq.org/topics/ocular-surface-and-contact-lens/)

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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.