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

Year Number of Results
1975 1
1977 3
1978 1
1980 1
1981 1
1984 2
1985 4
1986 1
1987 2
1988 5
1989 5
1990 2
1991 4
1992 10
1993 5
1994 3
1995 14
1996 4
1997 5
1998 9
1999 5
2000 4
2001 4
2002 6
2003 1
2004 3
2005 8
2006 9
2007 5
2008 4
2009 7
2010 1
2011 7
2012 9
2013 6
2014 8
2015 9
2016 14
2017 8
2018 10
2019 9
2020 9
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2022 8
2023 6
2024 2

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232 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
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.
These lesions are characterized by a relatively wide spectrum of morphological changes that may not be fully expressed, especially in the early stages of pregnancy. In addition, some changes can be observed in non-molar gravidities, which, unlike hydatidiform moles, lack a …
These lesions are characterized by a relatively wide spectrum of morphological changes that may not be fully expressed, especially in the ea …
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.
Each step has brought increased sensitivity to interrogate individual genomic variation in an unbiased method that does not require clinical prediction of the locus or loci involved. Notably, each step has also brought unique limitations in variant detection, for example, …
Each step has brought increased sensitivity to interrogate individual genomic variation in an unbiased method that does not require clinical …
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
In five sibships, simple aneuploidy in another pregnancy was observed, four of them being potentially viable. Two sisters had triploid conceptions. ...A frequency of almost 50% of mothers exposed to preconception abdominal radiation is suggestive of an association between …
In five sibships, simple aneuploidy in another pregnancy was observed, four of them being potentially viable. Two sisters had triploi …
Origin and ploidy of multipronuclear zygotes.
Tarin JJ, Trounson AO, Sathananthan H. Tarin JJ, et al. Reprod Fertil Dev. 1999;11(4-5):273-9. doi: 10.1071/rd99057. Reprod Fertil Dev. 1999. PMID: 10898292 Review.
Recently, several authors have proposed strategies for correction of triploidy based on the removal of the extra pronucleus at the zygote stage. ...In addition, although monospermic digynic zygotes have a single sperm centromere, which likely organizes a single bipolar spi …
Recently, several authors have proposed strategies for correction of triploidy based on the removal of the extra pronucleus at the zy …
Posttest risk calculation following positive noninvasive prenatal screening using cell-free DNA in maternal plasma.
Benn P. Benn P. Am J Obstet Gynecol. 2016 Jun;214(6):676.e1-7. doi: 10.1016/j.ajog.2016.01.003. Epub 2016 Jan 7. Am J Obstet Gynecol. 2016. PMID: 26772793 Review.
For example, commonly used rates for trisomy 13, monosomy-X, triploidy, and 22q11.2 deletion syndrome can vary by >4-fold and this can translate into large differences in PTR. ...
For example, commonly used rates for trisomy 13, monosomy-X, triploidy, and 22q11.2 deletion syndrome can vary by >4-fold and this …
Generation, genomic characterization, and differentiation of triploid human embryonic stem cells.
Haim-Abadi G, Golan-Lev T, Koren A, Benvenisty N. Haim-Abadi G, et al. Stem Cell Reports. 2023 May 9;18(5):1049-1060. doi: 10.1016/j.stemcr.2023.04.001. Epub 2023 Apr 27. Stem Cell Reports. 2023. PMID: 37116485 Free PMC article.
Humans are diploid organisms, and triploidy in human embryos is responsible for 10% of spontaneous miscarriages. ...This leads to a significant downregulation of cell surface ion channel genes, which are more essential in neural progenitors than in undifferentiated cells, …
Humans are diploid organisms, and triploidy in human embryos is responsible for 10% of spontaneous miscarriages. ...This leads to a s …
Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review.
Massalska D, Bijok J, Kucińska-Chahwan A, Zimowski JG, Ozdarska K, Raniszewska A, Panek GM, Roszkowski T. Massalska D, et al. Arch Gynecol Obstet. 2020 May;301(5):1139-1145. doi: 10.1007/s00404-020-05515-4. Epub 2020 Mar 26. Arch Gynecol Obstet. 2020. PMID: 32219520 Free PMC article. Review.
No case of proteinuria, preeclampsia or HELLP syndrome was observed. Only maternal complication observed in digynic triploidy was vaginal bleeding (50.0%). The mean time of beta-hCG normalization after diandric triploid pregnancies was 84 days (range 11-142 d …
No case of proteinuria, preeclampsia or HELLP syndrome was observed. Only maternal complication observed in digynic triploi
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 …
Molecular basis of clinical heterogeneity in neuroblastoma.
Brodeur GM, Nakagawara A. Brodeur GM, et al. Am J Pediatr Hematol Oncol. 1992 May;14(2):111-6. doi: 10.1097/00043426-199205000-00004. Am J Pediatr Hematol Oncol. 1992. PMID: 1356315 Review.
Recent studies suggest that these two features are related, and that the genotype frequently is predictive of response to treatment or the outcome of the patient. The genetic abnormalities that are characteristic of certain neuroblastomas include: (a) loss of heterozygosit …
Recent studies suggest that these two features are related, and that the genotype frequently is predictive of response to treatment o …
232 results