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BMC Medical Genomics|April 6, 2018
Genetic analysis of Wnt/PCP genes in neural tube defectsZhongzhong Chen, Yunping Lei, Xuanye Cao, et al.
American Journal of Medical Genetics. Part A|April 13, 2012
Gene variants in the folate-mediated one-carbon metabolism (FOCM) pathway as risk factors for conotruncal heart defectsHuiping Zhu, Wei Yang, Wei Lu, et al.
Animals : an Open Access Journal From MDPI|May 28, 2022
Characterization of Longitudinal Testosterone, Cortisol, and Musth in Male Asian Elephants (<i>Elephas maximus</i>), Effects of Aging, and Adrenal Responses to Social Changes and Health EventsSharon S Glaeser, Katie L Edwards, Stephen Paris, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 29, 2021
De novo ALX4 variant detected in child with non-syndromic craniosynostosisC S Fonteles, R H Finnell, Y Lei, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 13, 2011
Defective sumoylation pathway directs congenital heart diseaseJun Wang, Li Chen, Shu Wen, et al.
Molecular Genetics and Metabolism|January 27, 2004
Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defectsHuiping Zhu, Ned J Wicker, Kelly Volcik, et al.
ACS Chemical Biology|February 1, 2020
A Canstatin-Derived Peptide Provides Insight into the Role of Capillary Morphogenesis Gene 2 in Angiogenic Regulation and Matrix UptakeJordan G Finnell, Tsz-Ming Tsang, Lorna Cryan, et al.
Birth Defects Research|April 7, 2023
Neural tube defects: Prevalence, mortality, and maternal characteristics in two departmental hospitals in the northwestern region of Nicaragua, 2006-2018Dania María Pastora Bucardo, Fredman González, María Montes Pastora, et al.
International Journal of Nursing Education Scholarship|February 19, 2009
Survey on addictions: toward curricular change for family nurse practitionersNancy Campbell-Heider, Deborah S Finnell, Janice Cooke Feigenbaum, et al.
Oncotarget|September 15, 2017
A missense mutation in <i>TCN2</i> is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via MegalinPeiqiang Li, Lijuan Huang, Yufang Zheng, et al.
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