Pages that link to "Q73801654"
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The following pages link to Why are the genes that cause risk of human neural tube defects so hard to find? (Q73801654):
Displaying 13 items.
- Genetics of human neural tube defects (Q22337140) (← links)
- Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida (Q24632031) (← links)
- Stretching morphogenesis of the roof plate and formation of the central canal (Q27314877) (← links)
- Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3 (Q28507977) (← links)
- Gene expression profiling within the developing neural tube (Q35014706) (← links)
- Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10. (Q35447477) (← links)
- Localization of cartilage linking protein 1 during primary neurulation in the chick embryo (Q42438466) (← links)
- Alx3-deficient mice exhibit folic acid-resistant craniofacial midline and neural tube closure defects (Q43037401) (← links)
- Importance of model organisms in understanding the biology and genetic basis of human nonsyndromic neural tube defects. (Q43790116) (← links)
- Assessing the contributions of gene products to the form-shaping events of neurulation: a transgenic approach in chick. (Q52098318) (← links)
- Spina bifida (Q56168692) (← links)
- T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families (Q74457635) (← links)
- Symptomatic epilepsy with a tumor in the nose (Q79756330) (← links)