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Birth Defects Research|September 7, 2021
Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutationSuzanne Chartier, Lucile Boutaud, Edouard Le Guillou, et al.
Birth Defects Research|May 24, 2020
3-Methylglutaconic aciduria type VIII in an Indian neonateMalla Sadashivappa Sreedhara, Umamaheswari Balakrishnan, Prakash Amboiram, et al.
Birth Defects Research|May 28, 2020
Sinus pericranii, skull defects, and structural brain anomalies in TRAF7-related disorderAndrea Accogli, Marcello Scala, Marco Pavanello, et al.
Birth Defects Research|May 21, 2020
Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndromeGelila Yitsege, Bethany A Stokes, Julia A Sabatino, et al.
Birth Defects Research|June 25, 2020
Prenatal alcohol exposure induced congenital heart diseases: From bench to bedsideZhiyan Chen, Sheng Li, Linghong Guo, et al.
Birth Defects Research|November 10, 2022
Amelia and phocomelia in Finland: Characteristics and prevalences in a nationwide population-based studyNiklas Pakkasjärvi, Johanna Syvänen, Markus Wiro, et al.
Birth Defects Research|November 12, 2022
High-throughput detection of craniofacial defects in fluorescent zebrafishJoshua L Everson, Yung-Chia Tseng, Johann K Eberhart
Birth Defects Research|November 12, 2022
Validation of case definition algorithms for the ascertainment of congenital anomaliesYonabeth Nava de Escalante, Aanu Abayomi, Sylvie Langlois, et al.
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