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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1970 1
1973 1
1975 1
1977 1
1985 1
1989 1
1990 1
1991 3
1992 1
1993 2
1995 2
1996 2
1997 1
1999 1
2000 3
2001 1
2002 1
2005 1
2006 3
2007 2
2008 1
2009 1
2010 1
2011 2
2012 2
2013 1
2014 1
2015 2
2016 3
2017 3
2018 5
2019 9
2020 2
2021 2
2022 2
2023 1
2024 0

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60 results

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Page 1
Fetal fraction and noninvasive prenatal testing: What clinicians need to know.
Hui L, Bianchi DW. Hui L, et al. Prenat Diagn. 2020 Jan;40(2):155-163. doi: 10.1002/pd.5620. Epub 2019 Dec 10. Prenat Diagn. 2020. PMID: 31821597 Free PMC article. Review.
Clinicians need to understand the biological influences on FF to be able to provide optimal post-test counseling and clinical management. There are many different technologies available for the measurement of FF. ...In the meantime, having a "plan B" prepared for those pat …
Clinicians need to understand the biological influences on FF to be able to provide optimal post-test counseling and clinical managem …
Chromosomal microarray versus karyotyping for prenatal diagnosis.
Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, Savage M, Platt LD, Saltzman D, Grobman WA, Klugman S, Scholl T, Simpson JL, McCall K, Aggarwal VS, Bunke B, Nahum O, Patel A, Lamb AN, Thom EA, Beaudet AL, Ledbetter DH, Shaffer LG, Jackson L. Wapner RJ, et al. N Engl J Med. 2012 Dec 6;367(23):2175-84. doi: 10.1056/NEJMoa1203382. N Engl J Med. 2012. PMID: 23215555 Free PMC article. Clinical Trial.
Microarray analysis of the 4282 nonmosaic samples identified all the aneuploidies and unbalanced rearrangements identified on karyotyping but did not identify balanced translocations and fetal triploidy. In samples with a normal karyotype, microarray analysis revealed clin …
Microarray analysis of the 4282 nonmosaic samples identified all the aneuploidies and unbalanced rearrangements identified on karyotyping bu …
Prognostic impact of chromosomal abnormalities and copy number alterations in adult B-cell precursor acute lymphoblastic leukaemia: a UKALL14 study.
Moorman AV, Barretta E, Butler ER, Ward EJ, Twentyman K, Kirkwood AA, Enshaei A, Schwab C, Creasey T, Leongamornlert D, Papaemmanuil E, Patrick P, Clifton-Hadley L, Patel B, Menne T, McMillan AK, Harrison CJ, Rowntree CJ, Marks DI, Fielding AK. Moorman AV, et al. Leukemia. 2022 Mar;36(3):625-636. doi: 10.1038/s41375-021-01448-2. Epub 2021 Oct 16. Leukemia. 2022. PMID: 34657128 Free PMC article. Clinical Trial.
Patients with KMT2A-AFF1, complex karyotype (CK) and low hypodiploidy/near-triploidy (HoTr) had high relapse rates 50%, 60% & 53% and correspondingly poor survival. ...
Patients with KMT2A-AFF1, complex karyotype (CK) and low hypodiploidy/near-triploidy (HoTr) had high relapse rates 50%, 60% & 53% …
Distribution of diandric and digynic triploidy depending on gestational age.
Massalska D, Ozdarska K, Roszkowski T, Bijok J, Kucińska-Chahwan A, Panek GM, Zimowski JG. Massalska D, et al. J Assist Reprod Genet. 2021 Sep;38(9):2391-2395. doi: 10.1007/s10815-021-02202-4. Epub 2021 May 13. J Assist Reprod Genet. 2021. PMID: 33982170 Free PMC article. Clinical Trial.
PURPOSE: To establish the distribution of diandric and digynic triploidy depending on gestational age. METHODS: 107 triploid samples tested prospectively in a single genetic department during a four-year period were analyzed for parental origin of triploidy by Quant …
PURPOSE: To establish the distribution of diandric and digynic triploidy depending on gestational age. METHODS: 107 triploid samples …
24-chromosome PCR for aneuploidy screening.
Werner MD, Scott RT Jr, Treff NR. Werner MD, et al. Curr Opin Obstet Gynecol. 2015 Jun;27(3):201-5. doi: 10.1097/GCO.0000000000000167. Curr Opin Obstet Gynecol. 2015. PMID: 25699477 Review.
RECENT FINDINGS: The rigorous preclinical validation of quantitative real-time (q)PCR-based CCS involved an initial validation on cell lines, followed by a blinded evaluation on embryos. Comparison with alternative platforms and a prospective randomized clinical …
RECENT FINDINGS: The rigorous preclinical validation of quantitative real-time (q)PCR-based CCS involved an initial validation on cell lines …
Sphenofrontal distance in euploid and aneuploid fetuses.
Abele H, Sonek J, Goldschmid D, Wagner P, Hoopmann M, Kagan KO. Abele H, et al. Ultrasound Obstet Gynecol. 2017 Aug;50(2):187-191. doi: 10.1002/uog.17284. Epub 2017 Jul 9. Ultrasound Obstet Gynecol. 2017. PMID: 27550089 Free article.
METHODS: The database at our unit was searched to identify pregnancies with a diagnosis of trisomy 21, 18 or 13, triploidy or Turner syndrome after 15 weeks' gestation. Stored ultrasound images obtained between 19 and 22 weeks were reviewed. ...Only one (12.5%) fetus with …
METHODS: The database at our unit was searched to identify pregnancies with a diagnosis of trisomy 21, 18 or 13, triploidy or Turner …
First-trimester screening for trisomies 18 and 13, triploidy and Turner syndrome by detailed early anomaly scan.
Wagner P, Sonek J, Hoopmann M, Abele H, Kagan KO. Wagner P, et al. Ultrasound Obstet Gynecol. 2016 Oct;48(4):446-451. doi: 10.1002/uog.15829. Ultrasound Obstet Gynecol. 2016. PMID: 26611869 Free article.
The study population consisted of fetuses with trisomy 18, trisomy 13, triploidy or Turner syndrome. For each fetus with an abnormal karyotype, 50 randomly selected euploid fetuses were added to the study population. ...CONCLUSION: A detailed anomaly scan at 11-13 w …
The study population consisted of fetuses with trisomy 18, trisomy 13, triploidy or Turner syndrome. For each fetus with an abnormal …
Fetal exomphalos and chromosomal defects: relationship to maternal age and gestation.
Snijders RJ, Sebire NJ, Souka A, Santiago C, Nicolaides KH. Snijders RJ, et al. Ultrasound Obstet Gynecol. 1995 Oct;6(4):250-5. doi: 10.1046/j.1469-0705.1995.06040250.x. Ultrasound Obstet Gynecol. 1995. PMID: 8590187 Free article. Review.
In an ultrasound screening study involving 15,726 viable, singleton pregnancies at 11-14 weeks of gestation, exomphalos was diagnosed in 0.11% of the cases and, in those with exomphalos, the frequency of trisomy 18, trisomy 13 or triploidy was 61%. The corresponding freque …
In an ultrasound screening study involving 15,726 viable, singleton pregnancies at 11-14 weeks of gestation, exomphalos was diagnosed in 0.1 …
Hydatidiform molar pregnancy following assisted reproduction.
Nickkho-Amiry M, Horne G, Akhtar M, Mathur R, Brison DR. Nickkho-Amiry M, et al. J Assist Reprod Genet. 2019 Apr;36(4):667-671. doi: 10.1007/s10815-018-1389-9. Epub 2019 Jan 5. J Assist Reprod Genet. 2019. PMID: 30612209 Free PMC article.
The risk of recurrence of molar pregnancy following a previous molar was higher following ART compared to spontaneous conceptions. CONCLUSION: The use of ICSI should be protective against triploidy; however, the retrospective data suggests that molar pregnancy is not elimi …
The risk of recurrence of molar pregnancy following a previous molar was higher following ART compared to spontaneous conceptions. CONCLUSIO …
A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditions.
Xie P, Hu X, Kong L, Mao Y, Cheng D, Kang K, Dai J, Zhao D, Zhang Y, Lu N, Wan Z, Du R, Xiong B, Zhang J, Tan Y, Lu G, Gong F, Lin G, Liang B, Du J, Hu L. Xie P, et al. Hum Reprod. 2022 Oct 31;37(11):2546-2559. doi: 10.1093/humrep/deac190. Hum Reprod. 2022. PMID: 36066440
WIDER IMPLICATIONS OF THE FINDINGS: HaploPGT is an efficient and cost-effective detection platform with high clinical value for detecting genetic status. This platform could promote the application of PGT in ART, to increase pregnancy rate and decrease the birth of childre …
WIDER IMPLICATIONS OF THE FINDINGS: HaploPGT is an efficient and cost-effective detection platform with high clinical value for detec …
60 results