Cargando…
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
BACKGROUND: The aim of this study was to evaluate the best diagnostic approach for the genetic analysis of samples from first, second and third trimester intrauterine fetal deaths (IUFDs). We examined a total of 417 IUFD samples from fetuses with and without congenital anomalies. On 414 samples, kar...
Autores principales: | Kooper, Angelique JA, Faas, Brigitte HW, Feenstra, Ilse, de Leeuw, Nicole, Smeets, Dominique FCM |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906897/ https://www.ncbi.nlm.nih.gov/pubmed/24428858 http://dx.doi.org/10.1186/1755-8166-7-6 |
Ejemplares similares
-
Is routine karyotyping required in prenatal samples with a molecular or metabolic referral?
por: Kooper, Angelique JA, et al.
Publicado: (2012) -
Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study
por: Popescu-Hobeanu, Gabriela, et al.
Publicado: (2022) -
Usefulness of combined NGS and QF‐PCR analysis for product of conception karyotyping
por: Kato, Takema, et al.
Publicado: (2022) -
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) -
Ultrasound and echocardiographic findings obtained in the second and third trimesters of gestation in fetuses with normal karyotype and increased nuchal translucency
por: Moczulska, Hanna, et al.
Publicado: (2013)