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Birth Defects Research|March 15, 2024
Carbon monoxide affects early cardiac development in an avian modelFilipa Rombo Matias, Ian Groves, Joshua Durrans, et al.Birth Defects Research|April 2, 2024
Sex-dependent alterations of inflammatory factors, oxidative stress, and histopathology of the brain-gut axis in a VPA-induced autistic-like model of ratsZahra Salari, Amirhossein Moslemizadeh, Sara Sheibani Tezerji, et al.Birth Defects Research|September 12, 2024
Community-Engaged Research and the Use of Open Access ToxVal/ToxRef In Vivo Databases and New Approach Methodologies (NAM) to Address Human Health Risks From Environmental ContaminantsMarilyn Silva, Shosha Capps, Jonathan K LondonBirth Defects Research|September 17, 2024
Association Between Self-Reported Infections and Seropositivity Among Pregnant Women With Gastroschisis: A Case Control Study, With Emphasis on Chlamydia trachomatisM L Feldkamp, E Baum-Jones, E Y Enioutina, et al.Birth Defects Research|March 8, 2024
Human split hand/foot variants are not as functional as wildtype human PRDM1 in the rescue of craniofacial defectsBrittany T Truong, Lomeli C Shull, Bryan J Zepeda, et al.Birth Defects Research|February 27, 2024
Gastroschisis prevalence patterns in 27 surveillance programs from 24 countries, International Clearinghouse for Birth Defects Surveillance and Research, 1980-2017Marcia L Feldkamp, Mark A Canfield, Sergey Krikov, et al.Birth Defects Research|February 16, 2024
Updated EUROCAT guidelines for classification of cases with congenital anomaliesJorieke E H Bergman, Annie Perraud, Ingeborg Barišić, et al.Birth Defects Research|November 6, 2023
An epidemiologic study of penoscrotal transposition by maternal characteristics using data from the Texas birth defects registryRachel P Allred, Joanne Nguyen, A J Agopian, et al.Birth Defects Research|November 6, 2023
Risk of birth defects in pregnant persons with sleep-disordered breathing during pregnancyKatherine Pressman, Anthony M Kendle, Tara M Randis, et al.Birth Defects Research|October 6, 2023
SETting up the genome: KMT2D and KDM6A genomic function in the Kabuki syndrome craniofacial developmental disorderKarl B Shpargel, Gabrielle QuickstadPageof 120