<?xml version="1.0" encoding="UTF-8" ?>

    <journal>
    <language>en</language>
    <journal_id_issn>2008-2835</journal_id_issn>
    <journal_id_issn_online>2008-4625</journal_id_issn_online>
    <journal_id_pii></journal_id_pii>
    <journal_id_doi></journal_id_doi>
    <journal_id_isnet></journal_id_isnet>
    <journal_id_iranmedex>276</journal_id_iranmedex>
    <journal_id_magiran>5669</journal_id_magiran>
    <journal_id_sid>11181</journal_id_sid>
    <pubdate>
	    <type>gregorian</type>
	    <year>>2018</year>
	    <month>>July-September</month>
	    <day></day>
    </pubdate>
    <volume>10</volume>
    <number>3</number>
    <publish_type>online</publish_type>
    <publish_edition>1</publish_edition>
    <article_type>fulltext</article_type>
    <articleset>

<article>
	<language>en</language>
	<article_id_issn></article_id_issn>
	<article_id_issn_online></article_id_issn_online>
	<article_id_pubmed>30090211</article_id_pubmed>
	<article_id_pii></article_id_pii>
	<article_id_doi></article_id_doi>
	<article_id_iranmedex></article_id_iranmedex>
	<article_id_magiran></article_id_magiran>
	<article_id_sid></article_id_sid>
	<title_fa></title_fa>
	<title>Association of WNT3 Variations and Risk of Non-Syndromic Cleft Lip and Palate in a Population of Iranian Infants</title>
	<subject_fa></subject_fa>
	<subject></subject>
	<content_type_fa></content_type_fa>
	<content_type></content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;p&gt;Background: Nonsyndromic cleft lip and/or palate (NSCL/P) is the most common orofacial birth defect, often attributed to ethnic and environmental differences. Up to now, linkage analyses and genome-wide association studies have identified several genomic susceptibility regions for NSCL/P. The &lt;em&gt;WNT&lt;/em&gt; genes including &lt;em&gt;WNT3&lt;/em&gt; are strong candidates for NSCL/P, since they are involved in regulating mid-face development and upper lip fusion. This study tested association of the WNT3 polymorphisms, rs3809857 G/T and rs9890413 G/A, with the risk of NSCL/P in a population of Iranian infants.&lt;br /&gt;
Methods: The allelic and genotypic frequencies for each participant were determined in 113 unrelated Iranian subjects with NSCL/P and 220 control subjects using PCR and restriction fragment length polymorphism (RFLP) methods. A p-value of 0.05 was considered statistically significant.&amp;nbsp;&lt;br /&gt;
Results: The &lt;em&gt;WNT3&lt;/em&gt; rs3809857 GT genotype was significantly lower (p=0.039, OR=0.55, 95% CI=0.30-0.97) in the NSCL/P (21.2%) than the control group (30.42%). For the WNT3 rs9890413 G/A polymorphism, neither genotype nor allele frequencies were significantly different between the case and control groups.&lt;br /&gt;
Conclusion: Our results indicated that the &lt;em&gt;WNT3&lt;/em&gt; rs3809857 GT genotype may have a protective effect against NSCL/P in Iranian population.&lt;/p&gt;
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Genome wide association study, Cleft lip/palate, Polymorphism, WNT3</keyword>
	<start_page>168</start_page>
	<end_page>172</end_page>
	<web_url>https://www.ajmb.org/En/Article.aspx?id=323</web_url>
    <pdf_url>https://www.ajmb.org/PDF/En/FullText/323.pdf</pdf_url>
	<author_list><author><first_name>Homa</first_name><middle_name></middle_name><last_name>Farrokhi Karibozorg</last_name><suffix></suffix><affiliation>Department of Biochemistry, Islamic Azad University, Damghan Branch, Damghan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>91</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Nahid</first_name><middle_name></middle_name><last_name>Masoudian</last_name><suffix></suffix><affiliation>Department of Biochemistry, Islamic Azad University, Damghan Branch, Damghan, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>1298</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Kioomars</first_name><middle_name></middle_name><last_name>Saliminejad</last_name><suffix></suffix><affiliation>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>393</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Asghar</first_name><middle_name></middle_name><last_name>Ebadifar</last_name><suffix></suffix><affiliation>Dentofacial Deformities Research Center, Research Institute of Dental Sciences, Shahid Beheshti University of     Medical Sciences, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>891</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Koorosh</first_name><middle_name></middle_name><last_name>Kamali</last_name><suffix></suffix><affiliation>Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>89</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author><author><first_name>Hamid Reza</first_name><middle_name></middle_name><last_name>Khorram Khorshid</last_name><suffix></suffix><affiliation>Genetic Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran</affiliation><first_name_fa></first_name_fa><middle_name_fa></middle_name_fa><last_name_fa></last_name_fa><suffix_fa></suffix_fa><email></email><code>42</code><coreauthor></coreauthor><affiliation_fa></affiliation_fa></author></author_list>
</article>

</articleset>
</journal>

