Objectives Embryonic numerical and structural chromosomal abnormalities are the most
common cause of early pregnancy loss. However, the role of submicroscopic copy‐number …

Objective To characterize the types of genetic abnormalities and their prevalence in early
pregnancy loss at different developmental stages. We hypothesized that the prevalence of …

Objective To establish, based on a systematic literature review, the frequency of pathogenic
submicroscopic chromosomal aberrations in fetuses that are not at increased risk for …

Embryonic chromosomal abnormality is one of the significant causative factors of early
pregnancy loss. Our goal was to evaluate the clinical utility of next-generation sequencing …

A prospective analysis investigating the associations between pathogenic copy number
variations (pCNVs) and ultrasound soft markers (USMs) in fetuses and evaluating the …

Objectives To compare the performance of traditional G‐banding karyotyping with that of
copy number variation sequencing (CNV‐Seq) for detection of chromosomal abnormalities …

It is well established that embryonic chromosomal abnormalities (both in the number of
chromosomes and the structure) account for 50% of early pregnancy losses. However, little …

OBJECTIVE: To evaluate the association of other-than-common benign copy number
variants with specific fetal abnormalities detected by ultrasonogram. METHODS: Fetuses …

ABSTRACT OBJECTIVE To establish the prevalence of submicroscopic genetic copy
number variants (CNVs) in fetuses with a structural ultrasound anomaly (restricted to one …

Objective Chromosome aberrations are generally considered as one of the most substantial
causative factors contributing to spontaneous miscarriages. Cytogenetic analyses like G …