English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

recorded in spontaneous abortions and but with an extremely low incidence.1 Partial trisomy 17q is rare. Until now, 32 cases of partial trisomy for the distal region of 17q were reported either inherited or de novo.2-8 A derivative chromosome 4 due to partial trisomy of chromosome 17q has never been described, to our knowledge. We demonstrated that the fetus was a carrier of a de novo derivative chromosome 4 arising from partial trisomy 17q. Use of fluorescent in situ hybridization (FISH) analysis permitted the identification of the chromosome 17q breakpoint regions and confirmed the cytogenetic results.

türkiye klinikleri jinekoloji obstetrik

Prenatal Diagnosis of a De Novo Partial Trisomy 17q Case Associated with Increased Nuchal Translucency, Hypoplastic Left Heart Syndrome, Cerebral Anomalies: Case Report