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Maternal MTR genotype contributes to the risk of non‐syndromic cleft lip and palate in the Polish population
The aetiology of non‐syndromic cleft lip with or without cleft palate (CL/P) is very complex. It has been shown that polymorphic variants of genes encoding key proteins of folate and methionineExpand
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Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population.
BACKGROUND Cleft lip with or without cleft palate (CL/P) is one of the most common craniofacial malformations, with a complex and multifactorial etiology. Because of the genetic heterogeneity ofExpand
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Associations of folate and choline metabolism gene polymorphisms with orofacial clefts
Background Non-syndromic isolated cleft lip with or without cleft palate (NCL/P) is a common congenital anomaly in humans, the aetiology of which is complex and associated with both genetic andExpand
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Polymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the Polish population.
BACKGROUND Non-syndromic cleft lip and palate (CLP) is one of the most common birth defects. Recent genome-wide association studies (GWAS) have identified several novel risk loci associated with thisExpand
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Genotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palate.
The wingless-type MMTV integration site family (Wnt) signalling pathway plays a crucial role in craniofacial development. Recently, nucleotide variants in WNT genes have been shown to be associatedExpand
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Relation between the concentration of zinc in maternal whole blood and the risk of an infant being born with an orofacial cleft.
We investigated the relation between concentrations of maternal zinc and copper and the risk of an infant being born with an orofacial cleft. We did a case-control study using 116 mothers of childrenExpand
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Polymorphic variants of genes involved in homocysteine metabolism in celiac disease
Celiac disease (CD) is a polygenic chronic enteropathy conferring an increased risk for various nutrient deficiency states. Hyperhomocysteinemia is a frequent finding in CD and may be related to theExpand
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Nucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate
The CDH1 gene plays an important role during carcinogenesis and craniofacial morphogenesis. Germline mutations in this gene have been described in families presenting syndromic diffuse gastric cancerExpand
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[Vitamin E levels in patients with celiac disease].
BACKGROUND Coeliac disease (CD) is a genetically linked immune-mediated enteropathy triggered by the ingestion of gluten-containing grains food. Deficiencies of trace elements and vitamins may beExpand
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Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a Polish population.
BACKGROUND Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is one of the most common congenital anomalies, with a complex and still not fully understood etiology. Given the importantExpand
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