Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4.

Wolf-Hirschhorn syndrome is a clinically recognizable, multiple congenital anomaly syndrome usually associated with terminal deletion of the short arm of chromosome 4. A girl with clinical features of Wolf-Hirschhorn syndrome did not show an obvious deletion of chromosome 4, and a molecular defect w...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Altherr, M. R., Bengtsson, U., Elder, F. F., Ledbetter, D. H., Wasmuth, J. J., McDonald, M. E., Gusella, J. F., Greenberg, F.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Society of Human Genetics 1991
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC1702407/
https://ncbi.nlm.nih.gov/pubmed/1746553
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak