Results 121 to 130 of about 2,707,119 (197)

900: A pilot validation study for cell-based noninvasive prenatal testing (NIPT) in 42 cases [PDF]

American Journal of Obstetrics and Gynecology, 2019
Liesbeth Vossaert, Qun Wang, Roseen Salman, Anne McCombs, David Henke, Chunjing Qu, Weimin Bi, Brynn Levy, Yaping Yang, Chad Shaw, Ronald Wapner, Amy Breman, Ignatia Van den Veyver, Arthur Beaudet   +13 more
openaire   +1 more source

NIPT-based prenatal screening of maternal Xq28 copy number variations in a cohort of 80,371 pregnancies. [PDF]

Arch Gynecol Obstet
Meng L, Xu Y, Liang Y, Zhou R, Zhao J, Huo H, Zhang Q, Gao J, Liu T, Dai M, Du P, Wang Y, Hu P, Xu Z.   +13 more
europepmc   +1 more source

Selection and evaluation of DNase I hypersensitive sites for prenatal screening of trisomy 21 in the fetus. [PDF]

Vavilovskii Zhurnal Genet Selektsii
Mazur AM, Starshin AS, Bogush NV, Prokhortchouk EB.   +3 more
europepmc   +1 more source

Stratified obstetric management for heterogeneous rare diseases: a precision medicine framework based on four genetic archetypes. [PDF]

Front Med (Lausanne)
Lv S, Yang H, Cui Y, Yang H.
europepmc   +1 more source

Clinical application of fetal Nuchal Translucency combined with noninvasive prenatal testing in screening chromosome abnormalities. [PDF]

PLoS One
Fu G, Hu S.
europepmc   +1 more source

AI-guided meta-analysis of non-invasive prenatal testing platforms for trisomy 21 screening: comparative evaluation of cffDNA and fetal cell-based approaches. [PDF]

BMC Pregnancy Childbirth
Elmetwalli A, Ameen F, Magrashi N, Alamri ES, Albalawi AN, Alzahrani OR, El-Far AH.   +6 more
europepmc   +1 more source

Clinical Implications and Limitations of Noninvasive Prenatal Testing for Detecting Fetal Copy Number Variations: A Multicenter Study in Shaanxi Province, China. [PDF]

Med Sci Monit
Wang H, Zhang L, Yang T, Jia Y, Liu R, Jia Z, Liu Y, Bai G.   +7 more
europepmc   +1 more source

Technological Advances in Molecular Diagnostic Methods for Hereditary Diseases in Preconception and Prenatal Settings. [PDF]

Curr Issues Mol Biol
Kong D, Zhao J, Diao H, Qiu S, Peng Y, Liu T.   +5 more
europepmc   +1 more source

Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 16p13.11 microduplications. [PDF]

Medicine (Baltimore)
Xu T, Yue F, Ge Y, Liu R.
europepmc   +1 more source

Neonatal cytogenetic validation demonstrates high accuracy of single-nucleotide polymorphism-based non-invasive prenatal testing: a 4466-case single-center study. [PDF]

J Hum Genet
Uchida S, Mizuguchi Y, Sato S, Sueoka K, Tanaka M.   +4 more
europepmc   +1 more source