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Associations of folate and choline metabolism gene polymorphisms with orofacial cleftsCoeliac disease and birth defects in offspringA mutation in mouse Pak1ip1 causes orofacial clefting while human PAK1IP1 maps to 6p24 translocation breaking points associated with orofacial cleftingNucleotide variants of the cancer predisposing gene CDH1 and the risk of non-syndromic cleft lip with or without cleft palate.Malonylcarnitine in newborns with non-syndromic cleft lip with or without cleft palate.Nucleotide Variants of the BH4 Biosynthesis Pathway Gene GCH1 and the Risk of Orofacial Clefts.Analysis of the concentration of vitamin E in erythrocytes of patients with celiac disease.Stem cell regenerative therapy in alveolar cleft reconstruction.Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population.Association between polymorphisms at the GREM1 locus and the risk of nonsyndromic cleft lip with or without cleft palate in the Polish population.EVC gene polymorphisms and risks of isolated hypospadias - a preliminary study.Letter to the editor re: Comino, I., et al. Nutrients 2013, 5, 4250-4268.Polymorphic variants of genes related to arginine metabolism and the risk of orofacial clefts.Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts.Re: High serum levels of 8-hydroxy-2'-deoxyguanosine (8-OHdG) in mothers of children with cleft lip.Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate.Immune Abnormalities in Autism Spectrum Disorder-Could They Hold Promise for Causative Treatment?Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate.Nasolabial symmetry and aesthetics in children with complete unilateral cleft lip and palate.Genetic variants in BRIP1 (BACH1) contribute to risk of nonsyndromic cleft lip with or without cleft palate.Association of common variants in PAH and LAT1 with non-syndromic cleft lip with or without cleft palate (NSCL/P) in the Polish population.Further Evidence of the Association of the Diacylglycerol Kinase Kappa (DGKK) Gene With Hypospadias.Association of CDKAL1 nucleotide variants with the risk of non-syndromic cleft lip with or without cleft palate.Dental arch relationship in 5-year-olds with complete unilateral cleft lip and palate after early alveolar bone grafting.Addison's disease mimicking anorexia nervosaRe: Pregnancy outcomes in celiac womenEuropean "gluten-free" solid foods for infants may be a risky food for celiacsIs low male sex ratio in offspring of celiacs an advantage?Sex ratio variation in offspring of women with celiac diseaseCeliac disease presenting during puerperiumPolymorphic variants of genes encoding main antioxidant enzymes and the risk of CL/P-affected pregnanciesTherapeutic modalities for celiac diseaseHigh manganese levels in milk-based infant formulasA variable latent interval after exposure to gluten in persons developing celiac diseaseNeurological manifestations in celiacs and vitamin E statusPolymorphic variants at 10q25.3 and 17q22 loci and the risk of non-syndromic cleft lip and palate in the Polish populationGenotype and haplotype analysis of WNT genes in non-syndromic cleft lip with or without cleft palateMaternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish populationWhole blood propionylcarnitine in newborns with orofacial cleftLack of association of polymorphic variants of genes encoding zinc transporters with the risk of orofacial cleft-affected pregnancies
P50
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P50
description
researcher, ORCID id # 0000-0001-8606-2509
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wetenschapper
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name
K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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K Hozyasz
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P214
P106
P1153
7003307657
P214
P31
P496
0000-0001-8606-2509
P7859
viaf-311144484