# Annals of Human Genetics

**Type:** Journals  
**Canonical URL:** https://scholariq.org/journals/annals-of-human-genetics/

## Facts

| Field | Value |
| --- | --- |
| Open Access | false |
| ISSN-L | 0003-4800 |
| ISSNs | 0003-4800,1469-1809 |
| OpenAlex ID | https://openalex.org/S131700781 |
| Publisher | Wiley |

## Journal papers

- [Turner syndrome: a cytogenetic and molecular study](https://scholariq.org/papers/turner-syndrome-a-cytogenetic-and-molecular-study-2/)
- [Turner syndrome: a cytogenetic and molecular study](https://scholariq.org/papers/turner-syndrome-a-cytogenetic-and-molecular-study/)
- [Spectrum and Frequency of <i>SLC26A4</i> Mutations Among Czech Patients with Early Hearing Loss with and without Enlarged Vestibular Aqueduct (EVA)](https://scholariq.org/papers/spectrum-and-frequency-of-i-slc26a4-i-mutations-among-czech-patients-with-early/)
- [The Role of TLR4, TNF-α and IL-1β in Type 2 Diabetes Mellitus Development within a North Indian Population](https://scholariq.org/papers/the-role-of-tlr4-tnf-and-il-1-in-type-2-diabetes-mellitus-development-within-a/)
- [Clinical and molecular characterization of Indian patients with fructose‐1, 6‐bisphosphatase deficiency: Identification of a frequent variant (E281K)](https://scholariq.org/papers/clinical-and-molecular-characterization-of-indian-patients-with-fructose-1-6/)

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