المؤلفون: Yunping Lei, Huiping Zhu, Cody Duhon, Wei Yang, M Elizabeth Ross, Gary M Shaw, Richard H Finnell

المصدر: PLoS ONE, Vol 8, Iss 7, p e69262 (2013)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3724847?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/83129a6d3bf04ad9993699b99d5a5199

المؤلفون: Claudia J. Chapa, Philip J. Lupo, Huiping Zhu, Richard H. Finnell, Mark A. Canfield, Cody Duhon, Gary M. Shaw, Darryl Nousome

المصدر: Molecular Genetics and Metabolism. 107:592-595

مصطلحات موضوعية: Adult, Male, Risk, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Offspring, Endocrinology, Diabetes and Metabolism, GTP cyclohydrolase I, Gene Expression, Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Biochemistry, Article, Endocrinology, Surveys and Questionnaires, Internal medicine, Odds Ratio, Genetics, medicine, Humans, SNP, Neural Tube Defects, GTP Cyclohydrolase, Molecular Biology, Neural tube defect, biology, Haplotype, Infant, Newborn, Infant, Odds ratio, medicine.disease, Biopterin, United States, Haplotypes, Child, Preschool, Relative risk, biology.protein, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83dc326304ede6e5a6111bd4c966c61b
https://doi.org/10.1016/j.ymgme.2012.09.020

المؤلفون: Richard H. Finnell, Huiping Zhu, Cody Duhon, Gary M. Shaw, M. Elizabeth Ross, Wei Yang, Yunping Lei

المصدر: PLoS ONE, Vol 8, Iss 7, p e69262 (2013)
PLoS ONE

مصطلحات موضوعية: lcsh:Medicine, medicine.disease_cause, Madin Darby Canine Kidney Cells, Mice, 0302 clinical medicine, Missense mutation, lcsh:Science, Spinal Dysraphism, Conserved Sequence, Genetics, 0303 health sciences, Mutation, Multidisciplinary, Intracellular Signaling Peptides and Proteins, Cell Polarity, 3. Good health, Protein Transport, medicine.anatomical_structure, Protein Binding, Subcellular Fractions, Research Article, SCRIB, congenital, hereditary, and neonatal diseases and abnormalities, Molecular Sequence Data, Mutation, Missense, Biology, 03 medical and health sciences, Open Reading Frames, Dogs, Anencephaly, medicine, Craniorachischisis, Animals, Humans, Genetic Predisposition to Disease, Amino Acid Sequence, Gene, Genetic Association Studies, 030304 developmental biology, Spina bifida, Tumor Suppressor Proteins, lcsh:R, Neural tube, Infant, Membrane Proteins, medicine.disease, nervous system diseases, HEK293 Cells, lcsh:Q, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74689a453b93a9ebd5df5631a4bfe929
http://europepmc.org/articles/PMC3724847?pdf=render