Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1956 1
1958 1
1962 1
1963 3
1964 3
1965 2
1966 6
1967 7
1968 7
1969 5
1970 4
1971 15
1972 10
1973 13
1974 15
1975 94
1976 126
1977 155
1978 158
1979 247
1980 235
1981 265
1982 287
1983 333
1984 517
1985 616
1986 703
1987 722
1988 922
1989 1221
1990 1425
1991 1515
1992 1144
1993 579
1994 647
1995 657
1996 586
1997 660
1998 570
1999 568
2000 611
2001 645
2002 507
2003 561
2004 576
2005 624
2006 669
2007 697
2008 700
2009 647
2010 777
2011 884
2012 829
2013 826
2014 792
2015 703
2016 655
2017 644
2018 586
2019 522
2020 189
Text availability
Article attribute
Article type
Publication date

Search Results

27,331 results
Results by year
Filters applied: . Clear all
Page 1
Should embryos with autosomal monosomy by preimplantation genetic testing for aneuploidy be transferred?: Implications for embryo selection from a systematic literature review of autosomal monosomy survivors.
Bunnell ME, Wilkins-Haug L, Reiss R. Bunnell ME, et al. Prenat Diagn. 2017 Dec;37(13):1273-1280. doi: 10.1002/pd.5185. Prenat Diagn. 2017. PMID: 29164644 Review.
RESULTS: Fifty-three reports describing 56 individuals with autosomal monosomy met the selection criteria: 1 case each of monosomy 14 and 16, 3 each for monosomy 15 and 18, 1 for group "E", 5 for monosomy 20, 24 for monosomy 21, 7 for monosom
RESULTS: Fifty-three reports describing 56 individuals with autosomal monosomy met the selection criteria: 1 case each of monosomy
3p deletion syndrome.
Kaur A, Khetarpal S. Kaur A, et al. Indian Pediatr. 2013 Aug;50(8):795-6. Indian Pediatr. 2013. PMID: 24036645 Free article.
Monosomy 18p is a risk factor for facioscapulohumeral dystrophy.
Balog J, Goossens R, Lemmers RJLF, Straasheijm KR, van der Vliet PJ, Heuvel AVD, Cambieri C, Capet N, Feasson L, Manel V, Contet J, Kriek M, Donlin-Smith CM, Ruivenkamp CAL, Heard P, Tapscott SJ, Cody JD, Tawil R, Sacconi S, van der Maarel SM. Balog J, et al. J Med Genet. 2018 Jul;55(7):469-478. doi: 10.1136/jmedgenet-2017-105153. Epub 2018 Mar 21. J Med Genet. 2018. PMID: 29563141 Free PMC article.
BACKGROUND: 18p deletion syndrome is a rare disorder caused by partial or full monosomy of the short arm of chromosome 18. Clinical symptoms caused by 18p hemizygosity include cognitive impairment, mild facial dysmorphism, strabismus and ptosis. ...
BACKGROUND: 18p deletion syndrome is a rare disorder caused by partial or full monosomy of the short arm of chromosome 18. Clinical s …
Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
Yu AC, Zambrano RM, Cristian I, Price S, Bernhard B, Zucker M, Venkateswaran S, McGowan-Jordan J, Armour CM. Yu AC, et al. Am J Med Genet A. 2017 Jun;173(6):1593-1600. doi: 10.1002/ajmg.a.38241. Epub 2017 Apr 25. Am J Med Genet A. 2017. PMID: 28440577
We propose that monosomy of this region represents a novel microdeletion syndrome. We recommend that individuals with 7p22.3p22.2 deletions should receive a developmental assessment and a thorough cardiac exam, with consideration of an echocardiogram, as part of their init …
We propose that monosomy of this region represents a novel microdeletion syndrome. We recommend that individuals with 7p22.3p22.2 del …
[18q-syndrome].
Ieshima A, Kubota N. Ieshima A, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):337-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057252 Review. Japanese. No abstract available.
Transcriptomic behavior of genes associated with chromosome 21 aneuploidies in early embryo development.
Sanchez-Ribas I, Diaz-Gimeno P, Sebastián-León P, Mercader A, Quiñonero A, Ballesteros A, Pellicer A, Domínguez F. Sanchez-Ribas I, et al. Fertil Steril. 2019 May;111(5):991-1001.e2. doi: 10.1016/j.fertnstert.2019.01.023. Epub 2019 Mar 25. Fertil Steril. 2019. PMID: 30922649
PATIENT(S): A total of 26 high-quality donated embryos from in vitro fertilization (IVF) patients: trisomy 21 (n = 8), monosomy 21 (n = 10), and euploid (n = 8) blastocysts. ...However, monosomy 21 is strongly transcriptionally affected because early development inv …
PATIENT(S): A total of 26 high-quality donated embryos from in vitro fertilization (IVF) patients: trisomy 21 (n = 8), monosomy 21 (n …
Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3.
Putra M, Surti U, Hu J, Steele D, Clemens M, Saller DN, Yatsenko SA, Rajkovic A. Putra M, et al. Am J Med Genet A. 2017 Dec;173(12):3153-3157. doi: 10.1002/ajmg.a.38497. Epub 2017 Oct 19. Am J Med Genet A. 2017. PMID: 29048729
Inverted isodicentric chromosome 21 is a rare form of chromosomal rearrangement that may result in trisomy 21; sometimes this rearrangement may also lead to segmental monosomy of the terminal long arm of chromosome 21. ...The resulting phenotype in this infant might be a c …
Inverted isodicentric chromosome 21 is a rare form of chromosomal rearrangement that may result in trisomy 21; sometimes this rearrangement …
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. Qi H, et al. Medicine (Baltimore). 2019 Apr;98(14):e15027. doi: 10.1097/MD.0000000000015027. Medicine (Baltimore). 2019. PMID: 30946338 Free PMC article.
RATIONALE: Monosomy 18p deletion syndrome refers to a rare chromosomal disorder resulting from the part deletion of the short arm of chromosome 18. ...CMA may be served as an effective tool for the diagnosis of prenatal monosomy 18p deletion syndrome diagnosis....
RATIONALE: Monosomy 18p deletion syndrome refers to a rare chromosomal disorder resulting from the part deletion of the short arm of …
Chromosomal DNA balance in human stem cell line 4BL.
Akopyan HR, Kushniruk VO, Mykytenko DO, Huleuk NL, Kremenskaya Y, Lukash LL. Akopyan HR, et al. Tsitol Genet. 2016 Jul-Aug;50(4):79-89. Tsitol Genet. 2016. PMID: 30480421 English, Russian.
To investigate the nature of monosomy of certain chromosomes the array CGH and FISH analyses have been used. The aberrations of chromosomes have been identified in all the cases of monosomies previously revealed by G-banding. ...The probable cause of the monosomi
To investigate the nature of monosomy of certain chromosomes the array CGH and FISH analyses have been used. The aberrations of chrom …
Puzzling pieces of chromosome 7 loss or deletion.
Schneider RK, Delwel R. Schneider RK, et al. Blood. 2018 Jun 28;131(26):2871-2872. doi: 10.1182/blood-2018-04-844746. Blood. 2018. PMID: 29954818 No abstract available.
27,331 results
Jump to page
Feedback