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Best matches for Chromosomal Abnormalities Through Amniocentesis:

Chromosomal mosaicism in the fetoplacental unit. Grati FR et al. Best Pract Res Clin Obstet Gynaecol. (2017)

Higher male prevalence of chromosomal mosaicism detected by amniocentesis. Lin CJ et al. Taiwan J Obstet Gynecol. (2018)

The prevalence of non-detectable chromosomal abnormalities by QF-PCR in amniocentesis for certain referral indications: experience at a mainland Chinese hospital. Liao C et al. Arch Gynecol Obstet. (2014)

Search results

Items: 1 to 20 of 3106


Lower detectability of non-invasive prenatal testing compared to prenatal diagnosis in high-risk pregnant women.

Wang J, Wang ZW, Zhou Q, Zhang B, Yin T, Yu B, Wang LL.

Ann Transl Med. 2019 Jul;7(14):319. doi: 10.21037/atm.2019.06.70.


The assessment of combined karyotype analysis and chromosomal microarray in pregnant women of advanced maternal age: a multicenter study.

Shi Y, Ma J, Xue Y, Wang J, Yu B, Wang T.

Ann Transl Med. 2019 Jul;7(14):318. doi: 10.21037/atm.2019.06.63.


Non-invasive cell-free fetal DNA testing: a multicenter follow-up study of 31515 singleton pregnancies in southeastern China.

Xu L, Huang H, Lin N, Wang Y, He D, Zhang M, Chen M, Chen L, Lin Y.

Ultrasound Obstet Gynecol. 2019 Jul 31. doi: 10.1002/uog.20416. [Epub ahead of print]


Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review.

Van den Veyver IB.

Prenat Diagn. 2019 Aug;39(9):666-678. doi: 10.1002/pd.5520. Epub 2019 Jul 28.


Simultaneous analysis of bisphenol A fractions in maternal and fetal compartments in early second trimester of pregnancy.

Zbucka-Krętowska M, Łazarek U, Miltyk W, Sidorkiewicz I, Pierzyński P, Milewski R, Wołczyński S, Czerniecki J.

J Perinat Med. 2019 Sep 25;47(7):765-770. doi: 10.1515/jpm-2019-0040.


The reproductive outcome of an infertile man with AZFc microdeletions, via intracytoplasmic sperm injection in a high-risk pregnancy: Case report and literature review.

Hu C, Liu X, Li L, Hu X, Zhu H, Geng D, Liu R, Wang R.

Medicine (Baltimore). 2019 Jul;98(28):e16358. doi: 10.1097/MD.0000000000016358. Review.


Fetal tricuspid regurgitation in second trimester of pregnancies at risk for fetal chromosomal defects.

Benchamanon R, Suwanrath C, Pranpanus S.

J Clin Ultrasound. 2019 Jul 7. doi: 10.1002/jcu.22753. [Epub ahead of print]


Subchromosomal anomalies in small for gestational-age fetuses and newborns.

Ma Y, Pei Y, Yin C, Jiang Y, Wang J, Li X, Li L, Kagan KO, Wu Q.

Arch Gynecol Obstet. 2019 Sep;300(3):633-639. doi: 10.1007/s00404-019-05235-4. Epub 2019 Jul 4.


Increased nuchal translucency: results from microarray and RASopathy disorders testing.

Sinajon P, Chitayat D, Roifman M, Wasim S, Carmona S, Ryan G, Noor A, Kolomietz E, Chong K.

Ultrasound Obstet Gynecol. 2019 May 22. doi: 10.1002/uog.20352. [Epub ahead of print]


Prenatal Sacrococcygeal Teratoma Diagnosed in a Fetus with Partial Trisomy 13q22.

Dalal SS, Berry T, Pimentel VM.

Case Rep Obstet Gynecol. 2019 Apr 7;2019:2892869. doi: 10.1155/2019/2892869. eCollection 2019.


[Exploration of the process of prenatal screening and diagnosis for women with advanced maternal age based on results of 351 cases of fetal chromosomal abnormalities].

Dong Y, Zhang M, Wang Y, Li S, Guan X, Lyu W.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):538-542. doi: 10.3760/cma.j.issn.1003-9406.2019.06.002. Chinese.


[Application of copy number variation sequencing for prenatal diagnosis in women at an advanced maternal age].

Wang J, Chen L, Zhou C, Wang L, Xie H, Xiao Y, Zhu H, Hu T, Zhang Z, Zhu Q, Chen X, Liu Z, Liu S, Wang H, Liu H.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):533-537. doi: 10.3760/cma.j.issn.1003-9406.2019.06.001. Chinese.


Prenatal diagnosis of de novo monosomy 18p deletion syndrome by chromosome microarray analysis: Three case reports.

Qi H, Zhu J, Zhang S, Cai L, Wen X, Zeng W, Tang G, Luo Y.

Medicine (Baltimore). 2019 Apr;98(14):e15027. doi: 10.1097/MD.0000000000015027.


First trimester combined screening in patients with systemic lupus erythematosus: impact of pre-analytical variables on risk assessment.

de Sousa MJR, Ribeiro R, Syngelaki A, Nicolaides KH.

Clin Rheumatol. 2019 May;38(5):1251-1255. doi: 10.1007/s10067-019-04525-1. Epub 2019 Mar 28.


Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene.

Sun M, Lou J, Li Q, Chen J, Li Y, Li D, Yuan H, Liu Y.

Taiwan J Obstet Gynecol. 2019 Mar;58(2):292-295. doi: 10.1016/j.tjog.2019.01.022.


Cytogenetic Analysis of Amniotic Fluid Cells in 4206 Cases of High-Risk Pregnant Women.

Li H, Li Y, Zhao R, Zhang Y.

Iran J Public Health. 2019 Jan;48(1):126-131.


[Prenatal diagnosis of monochorionic-diamniotic twins discordant for 45,X/46,XX mosaicism].

Hu J, Xi H, Ma N, Pang J, Luo Y, Jia Z, Wang H.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):260-262. doi: 10.3760/cma.j.issn.1003-9406.2019.03.017. Chinese.


Long-Term Outcome of Fetuses with Soft Marker and Without Genetic or Structural Abnormality.

Tosun M, Kurtoglu Ozdes E, Malatyalioglu E, Yavuz E, Celik H, Bildircin FD, Canga K, Kokcu A, Ogur G.

J Obstet Gynaecol India. 2019 Feb;69(1):56-61. doi: 10.1007/s13224-018-1094-8. Epub 2018 Feb 10.


Diagnosis and clinical delineation of mosaic tetrasomy 5p.

Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB.

Eur J Med Genet. 2019 Feb 21. pii: S1769-7212(19)30032-1. doi: 10.1016/j.ejmg.2019.02.006. [Epub ahead of print] Review.


Prenatal circulating microRNA signatures of foetal Down syndrome.

Zbucka-Kretowska M, Niemira M, Paczkowska-Abdulsalam M, Bielska A, Szalkowska A, Parfieniuk E, Ciborowski M, Wolczynski S, Kretowski A.

Sci Rep. 2019 Feb 20;9(1):2394. doi: 10.1038/s41598-018-35876-5.

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