Association between C677T and A1298C MTHFR gene polymorphism and nonsyndromic orofacial clefts in the Turkish population: a case-parent study
Two common MTHFR gene polymorphisms (C677T and A1298C) have been implicated in the etiology of nonsyndromic cleft lip/palate (nsCL/P). To investigate the genotype association among nsCL/P in the Turkish population, 56 case-parent trios were recruited into the study. Genotype frequencies were...
Saved in:
| Main Authors: | Aida Semiç-Jusufagiç, Rıfat Bircan, Özhan Çelebiler, Melike Erdim, Nurten Akarsu, Nursel H Elçioğlu |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Hacettepe University Institute of Child Health
2012-12-01
|
| Series: | The Turkish Journal of Pediatrics |
| Online Access: | https://turkjpediatr.org/article/view/1698 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Association of MTHFR C677T, MTHFR A1298C polymorphism in relation to patients with autism in Thi-Qar Governorate
by: Roaa M. Nashee, et al.
Published: (2024-06-01) -
Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population
by: Koray Boduroğlu, et al.
Published: (2005-10-01) -
MTHFR A1298C Polymorphism and Risk of Preeclampsia: A Meta-Analysis
by: Yong Hu, et al.
Published: (2023-12-01) -
Evaluation of the Role of Two SNPs in MTHFR Gene Polymorphisms (rs1801133) 677 C>T and (rs 1801131) 1298A>C with Homocysteine Level in Iraqi Patients with Chronic Kidney Disease
by: Saife AL-AHMER, et al.
Published: (2024-08-01) -
Hypercoagulability and the A1298C MTHFR Mutation: Case Series of Unexplained Pulmonary Embolism
by: Akshat Sahai, et al.
Published: (2025-05-01)