[HTML][HTML] Non-invasive prenatal testing, what patients do not learn, may be due to lack of specialist genetic training by gynecologists and obstetricians?

T Liehr - Frontiers in Genetics, 2021 - frontiersin.org
Platforms for “non-invasive prenatal testing”(NIPT), or also referred to as “non-invasive
prenatal screening”(NIPS) have been available for over 10 years, and are the most recent …

[HTML][HTML] Bio-analysis of Saliva Using Paper Devices and Colorimetric Assays

A Narasimhan, H Jain, K Muniandy… - Journal of Analysis and …, 2024 - Springer
In light of the evolving nature of various diseases, time becomes a crucial factor in diagnosis
and identifying the underlying causes. A point-of-care device provides a rapid diagnosis of a …

Prenatal detection and evaluation of differences of sex development: A qualitative interview study of parental perspectives and unmet needs

J Whitehead, J Hirsch, I Rosoklija… - Prenatal …, 2022 - Wiley Online Library
Objectives Prenatal diagnoses of differences of sex development (DSD) are increasing due
to availability of cell‐free DNA screening (cell‐free DNA screening (cfDNA)). This study …

Genome-wide genetic diversity and IBD analysis reveals historic dissemination routes of pear in China

X Chen, M Zhang, M Sun, Y Liu, S Li, B Song… - Tree Genetics & …, 2022 - Springer
Pear (Pyrus) is an important temperate fruit, which originates in the southwestern region of
China and has more than 3000 year's cultivation history. However, the historic routes of pear …

Metode molekularne dijagnostike u prenatalnoj medicini

L Zaninović, A Katušić Bojanac… - Medicina Fluminensis …, 2022 - hrcak.srce.hr
Sažetak Prenatalna medicina u smislu probira kromosomskih abnormalnosti fetusa nastala
je 70-ih godina prošlog stoljeća. U 21. stoljeću, s razvojem tehnologija napredne i brze …

[HTML][HTML] Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report

TM Ali, E Mateu-Brull, N Balaguer, C Dantas… - European Journal of …, 2021 - Springer
Background Since 2011, screening maternal blood for cell-free foetal DNA (cffDNA)
fragments has offered a robust clinical tool to classify pregnancy as low or high-risk for …

SÀNG LỌC TRƯỚC SINH KHÔNG XÂM LẤN NIPT VÀ ỨNG DỤNG TRÊN 7015 THAI PHỤ TẠI TRUNG TÂM XÉT NGHIỆM QUỐC TẾ GENTIS

CT Dương, VH Nguyễn, QV Nguyễn… - Tạp chí Y học Việt …, 2021 - tapchiyhocvietnam.vn
Tóm tắt Dị tật bẩm sinh là vấn đề toàn cầu ảnh hưởng nghiêm trọng tới chất lượng cuộc
sống. Trong số những nguyên nhân đã biết, bất thường di truyền là nguyên nhân phổ biến …