Yüklüyor......
Molecular characterization of patients with 18q23 deletions.
The 18q- syndrome is a deletion syndrome that is characterized by mental retardation, hearing loss, midfacial hypoplasia, growth deficiency, and limb anomalies. Most patients with this syndrome have deletions from 18q21-qter. We report on three patients with deletions of 18q23. A mother and daughter...
Kaydedildi:
Asıl Yazarlar: | , , , , , , |
---|---|
Materyal Türü: | Artigo |
Dil: | Inglês |
Baskı/Yayın Bilgisi: |
1997
|
Konular: | |
Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1712465/ https://ncbi.nlm.nih.gov/pubmed/9106532 |
Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|