<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>2</title>
<title_fa>1</title_fa>
<short_title>3</short_title>
<subject>Literature &amp; Humanities</subject>
<web_url>http://idai.ir</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>9</journal_id_issn>
<journal_id_issn_online>10</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>7</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>fa</language>
<pubdate>
	<type>jalali</type>
	<year>1390</year>
	<month>10</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2012</year>
	<month>1</month>
	<day>1</day>
</pubdate>
<volume>11</volume>
<number>11</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>fa</language>
	<article_id_doi></article_id_doi>
	<title_fa>Incidence assessment of MTHFR C677T and A1298C polymorphisms in Iranian non-syndromic cleft lip and/or palate patients</title_fa>
	<title></title>
	<subject_fa>کودکان</subject_fa>
	<subject>Pediatric Dentistry</subject>
	<content_type_fa>پژوهشي</content_type_fa>
	<content_type>Research</content_type>
	<abstract_fa>&lt;b&gt;
Background and aims&lt;/b&gt;. The aim of the present study is to determine the incidence of MTHFR C677 T and A1298C mutations in Iranian patients with cleft lip and/or cleft palate. &lt;div&gt;&lt;b&gt;Materials and methods&lt;/b&gt;. We screened 61 Iranian patients with cleft lip and/or cleft palate for mutations in the two alleles of MTHFR gene associated with cleft lip and/or palate: A1298C and C677T, using Polymerase Chain Reaction following by RFLP. &lt;div&gt;&lt;b&gt;Results.&lt;/b&gt; The 677T and 1298C homozygote genotypes showed a frequency of 36.1% and 11.4%, respectively. Combined genotype frequencies in newborns having oral clefts showed that the highest genotype was 677TT/1298AA (22.9%) and 677TT/1298CC genotypes were not observed. &lt;/div&gt;&lt;div&gt;&lt;b&gt;Conclusion.&lt;/b&gt; The results showed that 65.6% of all patients had at least one T mutant allele in C677T and 58.9% C mutant allele for A1298C. According to the frequencies of homozygosity of mutant alleles, it could be said that MTHFR genotype of 677TT shows a greater role in having oral clefts.&lt;/div&gt;&lt;hr&gt;&lt;p class=&quot;MsoNormal&quot; style=&quot;text-align: left direction: ltr unicode-bidi: embed&quot;&gt;&lt;b&gt;Source:
&lt;/b&gt;Journal of Dental Research, Dental Clinics, Dental Prospects &lt;/p&gt;

&lt;p class=&quot;MsoNormal&quot; style=&quot;text-align: left direction: ltr unicode-bidi: embed&quot;&gt;&lt;a href=&quot;http://dentistry.tbzmed.ac.ir/joddd/index.php/joddd/article/view/1685&quot; target=&quot;_blank&quot;&gt;&lt;font color=&quot;#0000ff&quot;&gt;Full
Text&lt;/font&gt;&lt;/a&gt;&lt;/p&gt;&lt;/div&gt;</abstract_fa>
	<abstract></abstract>
	<keyword_fa>A1298C, C677T, methylenetetrahydrofolate reductase, orofacial cleft, polymorphism</keyword_fa>
	<keyword></keyword>
	<start_page>0</start_page>
	<end_page>0</end_page>
	<web_url>http://idai.ir/browse.php?a_code=A-10-32-3323&amp;slc_lang=fa&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Asghar</first_name>
	<middle_name></middle_name>
	<last_name>Ebadifar</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>ebadifar@hbi.ir </email>
	<code>100319475328460015303</code>
	<orcid>100319475328460015303</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Dentofacial Deformities Research Center, Research Institute of Dental Sciences, Shahid Behehsti University of Medical Sciences,  Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Nazila</first_name>
	<middle_name></middle_name>
	<last_name>Ameli</last_name>
	<suffix></suffix>
	<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>100319475328460015304</code>
	<orcid>100319475328460015304</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dental School, Semnan University of Medical Sciences, Semnan, Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Hamidreza</first_name>
	<middle_name></middle_name>
	<last_name>KhorramKhorshid</last_name>
	<suffix></suffix>
	<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>100319475328460015305</code>
	<orcid>100319475328460015305</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Genetic Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mehdi</first_name>
	<middle_name></middle_name>
	<last_name>Salehi zienabadi</last_name>
	<suffix></suffix>
	<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>100319475328460015306</code>
	<orcid>100319475328460015306</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Dental School, Semnan university of Medical Sciences, Semnan, Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Kourosh</first_name>
	<middle_name></middle_name>
	<last_name>Kamali</last_name>
	<suffix></suffix>
	<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>100319475328460015307</code>
	<orcid>100319475328460015307</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Avicenna Research Institute, ACECR, Tehran, Iran</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Tayyebe</first_name>
	<middle_name></middle_name>
	<last_name>Khoshbakht</last_name>
	<suffix></suffix>
	<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>100319475328460015308</code>
	<orcid>100319475328460015308</orcid>
	<coreauthor>No</coreauthor>
	<affiliation> Genetic Research Centre, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
