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

Year Number of Results
1976 3
1977 2
1978 2
1981 1
1982 1
1983 3
1984 4
1985 2
1986 4
1987 3
1988 10
1989 14
1990 6
1991 6
1992 10
1993 6
1994 13
1995 18
1996 10
1997 12
1998 14
1999 8
2000 15
2001 10
2002 9
2003 7
2004 8
2005 15
2006 7
2007 14
2008 9
2009 19
2010 12
2011 16
2012 13
2013 10
2014 17
2015 15
2016 27
2017 17
2018 14
2019 16
2020 14
2021 11
2022 15
2023 11
2024 5

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446 results

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Page 1
Triploid pregnancy-Clinical implications.
Massalska D, Bijok J, Kucińska-Chahwan A, Zimowski JG, Ozdarska K, Panek G, Roszkowski T. Massalska D, et al. Clin Genet. 2021 Oct;100(4):368-375. doi: 10.1111/cge.14003. Epub 2021 Jun 1. Clin Genet. 2021. PMID: 34031868 Review.
Triploidy is a life-limiting genetic aberration resulting from an extra haploid set of chromosomes of paternal (diandric triploidy) or maternal origin (digynic triploidy). Triploidy affects around 1%-2% of all conceptions. The majority of cases is misc …
Triploidy is a life-limiting genetic aberration resulting from an extra haploid set of chromosomes of paternal (diandric triploidy …
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 …
Hydatidiform mole.
Daumová M, Hadravská Š, Putzová M. Daumová M, et al. Cesk Patol. 2023 Summer;59(2):50-54. Cesk Patol. 2023. PMID: 37468322 English.
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% …
Exencephaly-anencephaly Sequence.
Society for Maternal-Fetal Medicine; Monteagudo A. Society for Maternal-Fetal Medicine, et al. Am J Obstet Gynecol. 2020 Dec;223(6):B5-B8. doi: 10.1016/j.ajog.2020.08.176. Epub 2020 Nov 7. Am J Obstet Gynecol. 2020. PMID: 33168213 Review. No abstract available.
Where have all the trisomies gone?
Palomaki GE, Lambert-Messerlian GM, Haddow JE. Palomaki GE, et al. Am J Obstet Gynecol. 2016 Nov;215(5):583-587.e1. doi: 10.1016/j.ajog.2016.06.046. Am J Obstet Gynecol. 2016. PMID: 27793310
Screening via cfDNA detects more common chromosome abnormalities (eg, trisomy 21, sex trisomies). Sequential screening can identify other aneuploidies (eg, triploidy), as well as chromosome abnormalities associated with fetal structural abnormalities. ...
Screening via cfDNA detects more common chromosome abnormalities (eg, trisomy 21, sex trisomies). Sequential screening can identify other an …
Triploidy and chromosomes.
Uchida IA, Freeman VC. Uchida IA, et al. Am J Obstet Gynecol. 1985 Jan 1;151(1):65-9. doi: 10.1016/0002-9378(85)90426-0. Am J Obstet Gynecol. 1985. PMID: 3966508
A frequency of almost 50% of mothers exposed to preconception abdominal radiation is suggestive of an association between radiation and triploidy and requires further investigation....
A frequency of almost 50% of mothers exposed to preconception abdominal radiation is suggestive of an association between radiation and t …
Genome sequencing and implications for rare disorders.
Posey JE. Posey JE. Orphanet J Rare Dis. 2019 Jun 24;14(1):153. doi: 10.1186/s13023-019-1127-0. Orphanet J Rare Dis. 2019. PMID: 31234920 Free PMC article. Review.
Notably, each step has also brought unique limitations in variant detection, for example, the low sensitivity of ES for detection of triploidy, and of CMA for detection of copy neutral structural variants. ...
Notably, each step has also brought unique limitations in variant detection, for example, the low sensitivity of ES for detection of trip …
First trimester combined screening - focus on early biochemistry.
Tørring N. Tørring N. Scand J Clin Lab Invest. 2016 Oct;76(6):435-47. doi: 10.1080/00365513.2016.1200131. Epub 2016 Jul 12. Scand J Clin Lab Invest. 2016. PMID: 27403933 Review.
Improvements in the algorithm have extended the screening to include trisomy 21 in mono- and dichorionic twin pregnancies, trisomy 18, trisomy 13 and triploidy. The results from large databases have shown that the screening algorithms are efficient for a range of rare auto …
Improvements in the algorithm have extended the screening to include trisomy 21 in mono- and dichorionic twin pregnancies, trisomy 18, triso …
446 results