161 related articles for article (PubMed ID: 27606664)
1. Normal newborn with prenatal suspicion of X chromosome monosomy due to confined placental mosaicism.
Serapinas D; Bartkeviciene D; Valantinaviciene E; Machtejeviene E
Arch Argent Pediatr; 2016 Oct; 114(5):e362-5. PubMed ID: 27606664
[TBL] [Abstract][Full Text] [Related]
2. Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Examinations.
Libotte F; Carpineto SL; Dello Russo C; Viola A; Margiotti K; Restaldi F; Novelli A; Mesoraca A; Giorlandino C
J Med Life; 2020; 13(4):624-628. PubMed ID: 33456614
[TBL] [Abstract][Full Text] [Related]
3. A pregnancy with discordant fetal and placental chromosome 18 aneuploidies revealed by invasive and noninvasive prenatal diagnosis.
Chen C; Cram DS; Xie F; Wang P; Xu X; Li H; Song Z; Chen D; Zhang J; Tang S
Reprod Biomed Online; 2014 Jul; 29(1):136-9. PubMed ID: 24797099
[TBL] [Abstract][Full Text] [Related]
4. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy.
Rudd MK; Schleede JB; Williams SR; Lee K; Laffin J; Pasion R; Papenhausen PR
Prenat Diagn; 2018 Nov; 38(12):920-923. PubMed ID: 30156302
[TBL] [Abstract][Full Text] [Related]
5. Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes.
Lebo RV; Novak RW; Wolfe K; Michelson M; Robinson H; Mancuso MS
J Transl Med; 2015 Aug; 13():260. PubMed ID: 26260800
[TBL] [Abstract][Full Text] [Related]
6. Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Petersen AK; Cheung SW; Smith JL; Bi W; Ward PA; Peacock S; Braxton A; Van Den Veyver IB; Breman AM
Am J Obstet Gynecol; 2017 Dec; 217(6):691.e1-691.e6. PubMed ID: 29032050
[TBL] [Abstract][Full Text] [Related]
7. Maternal mosaicism of sex chromosome causes discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Wang L; Meng Q; Tang X; Yin T; Zhang J; Yang S; Wang X; Wu H; Shi Q; Jenkins EC; Zhong N; Gu Y
Taiwan J Obstet Gynecol; 2015 Oct; 54(5):527-31. PubMed ID: 26522104
[TBL] [Abstract][Full Text] [Related]
8. Discordance between ultrasound and cell free DNA screening for monosomy X.
Kagan KO; Hoopmann M; Singer S; Schaeferhoff K; Dufke A; Mau-Holzmann UA
Arch Gynecol Obstet; 2016 Aug; 294(2):219-24. PubMed ID: 27022934
[TBL] [Abstract][Full Text] [Related]
9. A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.
Li J; Xie M; Wang F; Ma J; Li J; Chen C; Li Z; Wang J; Zhang Y; Li Y
Mol Genet Genomic Med; 2020 Aug; 8(8):e1279. PubMed ID: 32463164
[TBL] [Abstract][Full Text] [Related]
10. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560
[TBL] [Abstract][Full Text] [Related]
11. Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome.
Dowlut-McElroy T; Davis S; Howell S; Gutmark-Little I; Bamba V; Prakash S; Patel S; Fadoju D; Vijayakanthi N; Haag M; Hennerich D; Dugoff L; Shankar RK
Am J Obstet Gynecol; 2022 Dec; 227(6):862-870. PubMed ID: 35841934
[TBL] [Abstract][Full Text] [Related]
12. Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.
Portnoï MF; Chantot-Bastaraud S; Christin-Maitre S; Carbonne B; Beaujard MP; Keren B; Lévy J; Dommergues M; Cabrol S; Hyon C; Siffroi JP
Eur J Med Genet; 2012 Nov; 55(11):635-40. PubMed ID: 22809487
[TBL] [Abstract][Full Text] [Related]
13. Abnormal non-invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotype.
Srebniak MI; Diderich KE; Noomen P; Dijkman A; de Vries FA; van Opstal D
Ultrasound Obstet Gynecol; 2014 Jul; 44(1):109-11. PubMed ID: 24585494
[TBL] [Abstract][Full Text] [Related]
14. Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome and a normal 46,XX karyotype at birth.
Chen CP
Taiwan J Obstet Gynecol; 2024 Jan; 63(1):118-119. PubMed ID: 38216249
[No Abstract] [Full Text] [Related]
15. Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling.
Gilbert B; Yardin C; Briault S; Belin V; Lienhardt A; Aubard Y; Battin J; Servaud M; Philippe HJ; Lacombe D
Prenat Diagn; 2002 Aug; 22(8):697-702. PubMed ID: 12210579
[TBL] [Abstract][Full Text] [Related]
16. Confirmatory testing illustrates additional risks for structural sex chromosome abnormalities in fetuses with a non-invasive prenatal screen positive for monosomy X.
Sund KL; Khattar D; Boomer T; Caldwell S; Dyer L; Hopkin RJ; Smolarek TA
Am J Med Genet C Semin Med Genet; 2020 Jun; 184(2):294-301. PubMed ID: 32476283
[TBL] [Abstract][Full Text] [Related]
17. Inconsistency between non-invasive prenatal testing (NIPT) and conventional prenatal diagnosis due to confined placental and fetal mosaicism: Two case reports.
Kang KM; Kim SH; Park JE; Kim H; Jang HY; Go M; Yang SH; Ryu SW; Bae SM; Cha DH; Shim SH
Front Med (Lausanne); 2022; 9():1063480. PubMed ID: 36590946
[TBL] [Abstract][Full Text] [Related]
18. Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing.
Wan J; Li R; Li F; Yu Q; Wang D; Sun X; Zhang Y; Jing X; Tang X; Chen G; Jiang F; Li F; Fu F; Li Y; Zhang L; Yi C; Li J; Li D; Liao C
J Matern Fetal Neonatal Med; 2022 Dec; 35(25):9647-9653. PubMed ID: 35282756
[TBL] [Abstract][Full Text] [Related]
19. Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Wang Y; Chen Y; Tian F; Zhang J; Song Z; Wu Y; Han X; Hu W; Ma D; Cram D; Cheng W
Clin Chem; 2014 Jan; 60(1):251-9. PubMed ID: 24193117
[TBL] [Abstract][Full Text] [Related]
20. Noninvasive prenatal testing (NIPT) detects variant of Turner syndrome not detectable by fluorescent
Eswarachari V; Kadam P; Movva S; Lingaiah S; Akther RM; Kidangan FX; Gowda KC; Golakoti RRK; Lall M; Mahajan S; Saviour P; Puri R; Verma IC; Vedam RL
J Matern Fetal Neonatal Med; 2019 Dec; 32(24):4177-4180. PubMed ID: 29793366
[No Abstract] [Full Text] [Related]
[Next] [New Search]
