Cargando…
Digynic triploidy: utility and challenges of noninvasive prenatal testing
Low fraction fetal DNA in noninvasive prenatal testing in the context of fetal growth restriction and multiple congenital anomalies should alert medical professionals to the possibility of digynic triploidy. Single-nucleotide polymorphism microarray can detect the parental origin of triploidy and ex...
Autores principales: | Fleischer, Julie, Shenoy, Archana, Goetzinger, Katherine, Cottrell, Catherine E, Baldridge, Dustin, White, Frances V, Shinawi, Marwan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4498852/ https://www.ncbi.nlm.nih.gov/pubmed/26185638 http://dx.doi.org/10.1002/ccr3.247 |
Ejemplares similares
-
Prenatal diagnosis of syndromic alobar holoprosencephaly associated with digynic triploidy fetus
por: Albu, Cristina-Crenguţa, et al.
Publicado: (2020) -
Distribution of diandric and digynic triploidy depending on gestational age
por: Massalska, Diana, et al.
Publicado: (2021) -
Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy
por: Fatemi, Nayeralsadat, et al.
Publicado: (2021) -
Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy
por: Kolarski, Milenko, et al.
Publicado: (2017) -
Prenatal Diagnosis of Triploidy in Fetus with Unexpected Chromosomal Translocation of Maternal Origin
por: Jadhav, Ajinkya, et al.
Publicado: (2023)