Investigation of FGF1 and FGFR gene polymorphisms in a group of Iranian patients with nonsyndromic cleft lip with or without cleft palate
β Scribed by Rafiqdoost, Zahra; Rafiqdoost, Amir; Rafiqdoost, Houshang; Hashemi, Mohammad; Khayatzadeh, Jina; Eskandari-Nasab, Ebrahim
- Book ID
- 122239525
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 814 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0165-5876
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## Background: Nonsyndromic cleft lip with or without cleft palate (cl/p) is a common complex birth defect caused by the interaction between multiple genes and environmental factors. ## Methods: Five hundred and eighty-seven single nucleotide polymorphisms in 40 candidate genes related to orofaci
## Abstract **BACKGROUND:** Nonsyndromic cleft lip with or without cleft palate (NCL/P) is a common structural malformation with a complex and multifactorial etiology. It has been shown that maternal psychological stress in the periconceptional period can contribute to an increase in the risk of NC