Pages that link to "Q42638450"
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The following pages link to Folate pathway gene alterations in patients with neural tube defects (Q42638450):
Displaying 16 items.
- Towards a cellular and molecular understanding of neurulation (Q28190887) (← links)
- Gene conversion causing human inherited disease: evidence for involvement of non-B-DNA-forming sequences and recombination-promoting motifs in DNA breakage and repair (Q30491768) (← links)
- Novel folate binding protein-1 interactions in embryonic orofacial tissue (Q33521602) (← links)
- Genetic and epigenetic contributions to human nutrition and health: managing genome-diet interactions (Q33647210) (← links)
- Genome-wide identification of pseudogenes capable of disease-causing gene conversion. (Q34521369) (← links)
- Gene conversion: mechanisms, evolution and human disease (Q34685613) (← links)
- Chromosomal abnormalities associated with neural tube defects (II): partial aneuploidy (Q37053299) (← links)
- Gene-nutrient interactions: importance of folic acid and vitamin B12 during early embryogenesis (Q37246148) (← links)
- The Rate and Tract Length of Gene Conversion between Duplicated Genes (Q37584974) (← links)
- Pseudogenes and their composers: delving in the 'debris' of human genome (Q38125345) (← links)
- Y chromosome palindromes and gene conversion (Q39183110) (← links)
- SNPs in the CpG island of NAP1L2: a possible link between DNA methylation and neural tube defects? (Q40718454) (← links)
- Reduced folate carrier polymorphism (80A-->G) and neural tube defects (Q44389085) (← links)
- Methylmalonic acid in amniotic fluid and maternal urine as a marker for neural tube defects (Q45021036) (← links)
- Purifying selection against gene conversions in the folate receptor genes of primates (Q46976145) (← links)
- Lack of association between folate receptor autoantibodies and conotruncal congenital heart defects (Q47232486) (← links)