Cargando…
Why Do Parents Prefer to Know the Fetal Sex as Part of Invasive Prenatal Testing?
Objectives. The aim of this study was to determine whether prospective parents, primarily referred for prenatal diagnosis to exclude Down syndrome, prefer to know the fetal sex as part of invasive testing. Methods. In this prospective study 400 pregnant women undergoing amniocentesis were invited to...
Autores principales: | Kooper, Angelique J. A., Pieters, Jacqueline J. P. M., Eggink, Alex J., Feuth, Ton B., Feenstra, Ilse, Wijnberger, Lia D. E., Rijnders, Robbert J. P., Quartero, Rik W. P., Boekkooi, Peter F., van Vugt, John M. G., Smits, Arie P. T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scholarly Research Network
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530785/ https://www.ncbi.nlm.nih.gov/pubmed/23304540 http://dx.doi.org/10.5402/2012/524537 |
Ejemplares similares
-
Women's Attitudes towards the Option to Choose between Karyotyping and Rapid Targeted Testing during Pregnancy
por: Kooper, Angelique J. A., et al.
Publicado: (2013) -
Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?
por: Kooper, Angelique JA, et al.
Publicado: (2012) -
Incidental Prenatal Diagnosis of Sex Chromosome Aneuploidies: Health, Behavior, and Fertility
por: Pieters, J. J. P. M., et al.
Publicado: (2011) -
Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis
por: Kooper, Angelique JA, et al.
Publicado: (2014) -
Prenatal identification of an inverted duplicated 13q marker chromosome with a neocentromere
por: van der Laan, Liselot, et al.
Publicado: (2023)