Yüklüyor......

29. No association between MTHFR C677T polymorphism and congenital heart disease in Saudi Arabian population

Congenital heart diseases (CHD) are the most common birth defects in the world. It is a major cause of childhood mortality and morbidity worldwide with about 7 per 1000 live birth. Studies suggest that Methylenetetrahydrofolate reductase (MTHFR) polymorphism C667T has been associated with congenital...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: S. Justin Carlus, Lama M. El-Attar, Sahar A.F. Hammoudah, Ghadeer Saleh Mossad Al Harbi, Ibrahim S. Almuzainy, Atiyeh Abdallah, Khalid Al Harbi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Saudi Heart Association 2015-10-01
Seri Bilgileri:Journal of the Saudi Heart Association
Online Erişim:http://www.sciencedirect.com/science/article/pii/S1016731515002699
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!