Wird geladen...
A locus for hereditary hypotrichosis localized to human chromosome 18q21.1
Hereditary hypotrichosis is a rare autosomal recessive condition characterized clinically by alopecia. Three consanguineous kindreds with multiple affected individuals were ascertained from different regions of Pakistan. A novel hypotrichosis locus was mapped to a 5.5 cM region on chromosome 18q21.1...
Gespeichert in:
| Veröffentlicht in: | Eur J Hum Genet |
|---|---|
| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2003
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6157268/ https://ncbi.nlm.nih.gov/pubmed/12891384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/sj.ejhg.5201005 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|