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abnormal finding in prenatal screening相关文献:
Practice Bulletin No. 187: Neural Tube Defects.
[No authors listed]
Obstet Gynecol. 2017 Dec;130(6):e279-e290. doi: 10.1097/AOG.0000000000002412.
PMID:29189693
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, Breman A, Xia F, Yang Y, Purgason A, Pourpak A, Chen Z, Wang X, Wang Y, Kulkarni S, Choy KW, Wapner RJ, Van den Veyver IB, Beaudet A, Parmar S, Wong LJ, Eng CM.
Nat Med. 2019 Mar;25(3):439-447. doi: 10.1038/s41591-018-0334-x. Epub 2019 Jan 28.
PMID:30692697
Routine 36-week scan: diagnosis of fetal abnormalities.
Syngelaki A, Mitsigiorgi R, Goadsby J, Hamed K, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol. 2025 Apr;65(4):427-435. doi: 10.1002/uog.29218. Epub 2025 Mar 25.
PMID:40131231
Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases.
Qin Y, Yao Y, Liu N, Wang B, Liu L, Li H, Gao T, Xu R, Wang X, Zhang F, Song J.
BMC Med Genomics. 2023 Oct 25;16(1):262. doi: 10.1186/s12920-023-01697-3.
PMID:37880672
Diagnosis of fetal non-chromosomal abnormalities on routine ultrasound examination at 11-13 weeks' gestation.
Syngelaki A, Hammami A, Bower S, Zidere V, Akolekar R, Nicolaides KH.
Ultrasound Obstet Gynecol. 2019 Oct;54(4):468-476. doi: 10.1002/uog.20844.
PMID:31408229
Prenatal screening in Jewish law.
Brown J.
J Med Ethics. 1990 Jun;16(2):75-80. doi: 10.1136/jme.16.2.75.
PMID:2195172
[Fetal MRI].
Blondin D, Turowski B, Schaper J.
Rofo. 2007 Feb;179(2):111-8. doi: 10.1055/s-2006-927307.
PMID:17310442
How far can prenatal screening go in preventing birth defects?
Savitz DA.
J Pediatr. 2008 Jan;152(1):3-4. doi: 10.1016/j.jpeds.2007.09.012.
PMID:18154886
Association between chromosome abnormities and prenatal diagnosis indicators screening in the second trimester of pregnancy.
Pan C, Li Z, Cheng G, Luo X, Nie F, Gao J, Yang P.
Medicine (Baltimore). 2023 Sep 1;102(35):e34762. doi: 10.1097/MD.0000000000034762.
PMID:37657051
Prenatal cfDNA Screening for Emanuel Syndrome and Other Unbalanced Products of Conception in Carriers of the Recurrent Balanced Translocation t(11;22): One Laboratory's Retrospective Experience.
Soster E, Dyr B, Caldwell S, Sussman A, Magharyous H.
Genes (Basel). 2023 Oct 10;14(10):1924. doi: 10.3390/genes14101924.
PMID:37895273
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