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References
- Borrell A, Grande M, Pauta M, Rodriguez-Revenga L, Figueras F. 2018. Chromosomal microarray analysis in fetuses with growth restriction and normal karyotype: a systematic review and meta-analysis. Fetal Diagnosis and Therapy 44:1–9.
- de Wit MC, Srebniak MI, Joosten M, Govaerts LC, Kornelisse RF, Papatsonis DN, et al. 2017. Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18–24 weeks. Ultrasound in Obstetrics & Gynecology 49:342–348.
- Dupré T, Vuillaumier-Barrot S, Chantret I, Sadou Yayé H, Le Bizec C, Afenjar A, et al. 2010. Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations. Journal of Medical Genetics 47:729–735.
- International Society for Prenatal Diagnosis; Society for Maternal and Fetal Medicine; Perinatal Quality Foundation. 2018. Joint Position Statement from the International Society for Prenatal Diagnosis (ISPD), the Society for Maternal Fetal Medicine (SMFM), and the Perinatal Quality Foundation (PQF) on the use of genome-wide sequencing for fetal diagnosis. Prenatal Diagnosis 38:6–9.
- Ng BG, Shiryaev SA, Rymen D, Eklund EA, Raymond K, Kircher M, et al. 2016. ALG1-CDG: clinical and molecular characterization of 39 unreported patients. Human Mutation 37:653–660.
- Schwarz M, Thiel C, Lübbehusen J, Dorland B, de Koning T, von Figura K, et al. 2004. Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik. American Journal of Human Genetics 74:472–481.
- Soehn AS, Rattay TW, Beck-Wödl S, Schäferhoff K, Monk D, Döbler-Neumann M, et al. 2016. Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 families. Neurology 87:186–191.
- Unterscheider J, Daly S, Geary MP, Kennelly MM, McAuliffe FM, O'Donoghue K, et al. 2013. Optimizing the definition of intrauterine growth restriction: the multicenter prospective PORTO Study. American Journal of Obstetrics and Gynecology 208:290.e1.
- Yamazawa K, Ogata T, Ferguson-Smith AC. 2010. Uniparental disomy and human disease: an overview. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics 154C:329–334.