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
1968 2
1970 2
1971 2
1972 1
1973 3
1974 1
1975 6
1976 7
1977 7
1978 8
1979 11
1980 3
1981 12
1983 1
1984 1
1985 3
1986 11
1987 5
1988 4
1989 5
1990 11
1991 9
1992 4
1993 7
1994 6
1995 8
1996 9
1997 3
1998 8
1999 4
2000 8
2001 9
2002 2
2003 8
2004 10
2005 6
2006 10
2007 7
2008 5
2009 5
2010 9
2011 4
2012 5
2013 10
2014 7
2015 5
2016 5
2017 5
2018 10
2019 8
2020 8
Text availability
Article attribute
Article type
Publication date

Search Results

295 results
Results by year
Filters applied: . Clear all
Page 1
Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2019 Sep;58(5):692-697. doi: 10.1016/j.tjog.2019.07.020. Taiwan J Obstet Gynecol. 2019. PMID: 31542095 Free article. Review.
Repeat amniocentesis at 22 weeks of gestation using uncultured amniocytes revealed an aCGH result of arr 22q11.1q13.33 (17,397,498-51,178,264) × 2.8 compatible with 80% mosaicism for trisomy 22, and a fluorescence in situ hybridization (FISH) result of mosaic …
Repeat amniocentesis at 22 weeks of gestation using uncultured amniocytes revealed an aCGH result of arr 22q11.1q13.33 (17,397,498-51 …
Trisomy 22 mosaicism and normal developmental outcome: report of two patients and review of the literature.
Abdelgadir D, Nowaczyk MJ, Li C. Abdelgadir D, et al. Am J Med Genet A. 2013 May;161A(5):1126-31. doi: 10.1002/ajmg.a.35812. Epub 2013 Mar 25. Am J Med Genet A. 2013. PMID: 23529842 Review.
In review of the literature, prenatal and postnatal growth failures were the most common complications of mosaic trisomy 22. ...It is conceivable that children with trisomy 22 mosaicism, with minimal physical findings and normal development are under d …
In review of the literature, prenatal and postnatal growth failures were the most common complications of mosaic trisomy 22. . …
Trisomy 22 with long spina bifida occulta: A case report.
Ma L, Ouyang Y, Qi Q, Hao N, Zhao D, Jiang Y, Meng H. Ma L, et al. Medicine (Baltimore). 2018 Sep;97(39):e12306. doi: 10.1097/MD.0000000000012306. Medicine (Baltimore). 2018. PMID: 30278506 Free PMC article.
INTRODUCTION: Complete non-mosaic trisomy 22 is a fatal chromosomal disorder that only few fetuses can survive over 12 weeks as reported. ...CONCLUSIONS: This was the first time a case of spinal cord defect was reported in trisomy 22 fetuses. More atte …
INTRODUCTION: Complete non-mosaic trisomy 22 is a fatal chromosomal disorder that only few fetuses can survive over 12 weeks a …
Tissue Specificity in Trisomy 22 Mosaicism: A Tale of Caution for Interpretation of Chromosomal Microarray Results.
Covington JD, Campbell C, Burke LW, Gardner JA. Covington JD, et al. J Assoc Genet Technol. 2018;44(4):137-140. J Assoc Genet Technol. 2018. PMID: 30521494
Trisomy 22 is the second most common aneuploidy in spontaneous miscarriages and has a nondescript and variable phenotype, especially in cases of mosaicism. ...Diagnoses such as mosaic trisomy 22 suggest the second tier of testing in undiagnosed cases s
Trisomy 22 is the second most common aneuploidy in spontaneous miscarriages and has a nondescript and variable phenotype, espe
Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report.
Kalayinia S, Shahani T, Biglari A, Maleki M, Rokni-Zadeh H, Razavi Z, Mahdieh N. Kalayinia S, et al. J Clin Lab Anal. 2019 Feb;33(2):e22663. doi: 10.1002/jcla.22663. Epub 2018 Sep 26. J Clin Lab Anal. 2019. PMID: 30259573
BACKGROUND: Trisomy 22 mosaicism is a rare autosomal anomaly with survival compatibility. Recognition of the complete trisomy 22 which is incompatible with life from the mosaic form is critical for genetic counseling. ...We describe a 4-year-old boy wi …
BACKGROUND: Trisomy 22 mosaicism is a rare autosomal anomaly with survival compatibility. Recognition of the complete triso
Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W. Chen CP, et al. Taiwan J Obstet Gynecol. 2017 Oct;56(5):691-693. doi: 10.1016/j.tjog.2017.09.001. Taiwan J Obstet Gynecol. 2017. PMID: 29037560 Free article.
OBJECTIVE: We present the application of non-invasive prenatal testing (NIPT) in late gestation in a pregnancy associated with intrauterine growth restriction (IUGR) and trisomy 22 confined placental mosaicism (CPM). ...CVS revealed a karyotype of 47,XY,+22 i …
OBJECTIVE: We present the application of non-invasive prenatal testing (NIPT) in late gestation in a pregnancy associated with intrauterine …
Trisomy 22.
Zellweger H, Ionasescu V, Simpson J. Zellweger H, et al. J Genet Hum. 1975 Mar;23(1):65-75. J Genet Hum. 1975. PMID: 1165480
Trisomy 22 is much rarer than trisomy 21. This report presents presumptive evidence that the cat eye syndrome (CES), the so-called "trisomy 22" (T22), the intermediate cases (IM) with cardinal symptoms of CES and T22, and some cases of mental re
Trisomy 22 is much rarer than trisomy 21. This report presents presumptive evidence that the cat eye syndrome (CES), th
Rare autosomal trisomies: Important and not so rare.
Scott F, Bonifacio M, Sandow R, Ellis K, Smet ME, McLennan A. Scott F, et al. Prenat Diagn. 2018 Sep;38(10):765-771. doi: 10.1002/pd.5325. Epub 2018 Jul 17. Prenat Diagn. 2018. PMID: 29956348
RESULTS: There were 28 RATs identified in 23 388 samples (one in 835), the most common being trisomy 7 (n = 6), followed by trisomy 16 (n = 4) and trisomy 22 (n = 3). ...Pregnancy outcomes varied by chromosome being generally favourable for some (eg, …
RESULTS: There were 28 RATs identified in 23 388 samples (one in 835), the most common being trisomy 7 (n = 6), followed by trisom
Live-born trisomy 22: patient report and review.
Heinrich T, Nanda I, Rehn M, Zollner U, Frieauff E, Wirbelauer J, Grimm T, Schmid M. Heinrich T, et al. Mol Syndromol. 2013 Jan;3(6):262-9. doi: 10.1159/000346189. Epub 2013 Jan 11. Mol Syndromol. 2013. PMID: 23599696 Free PMC article.
Trisomy 22 is a common trisomy in spontaneous abortions. In contrast, live-born trisomy 22 is rarely seen due to severe organ malformations associated with this condition. Here, we report on a male infant with complete, non-mosaic trisomy
Trisomy 22 is a common trisomy in spontaneous abortions. In contrast, live-born trisomy 22 is rarely seen
Co-occurrence of non-mosaic trisomy 22 and inherited balanced t(4;6)(q33;q23.3) in a liveborn female: case report and review of the literature.
Kehinde FI, Anderson CE, McGowan JE, Jethva RN, Wahab MA, Glick AR, Sterner MR Jr, Pascasio JM, Punnett HH, Liu J. Kehinde FI, et al. Am J Med Genet A. 2014 Dec;164A(12):3187-93. doi: 10.1002/ajmg.a.36778. Epub 2014 Sep 24. Am J Med Genet A. 2014. PMID: 25257307 Review.
Trisomy 22 is the third most common autosomal trisomy occurring in about 0.4% of all clinically recognized pregnancies. Complete non-mosaic trisomy 22 is extremely rare in live births. ...In addition, she had lobar holoprosencephaly, aqueductal
Trisomy 22 is the third most common autosomal trisomy occurring in about 0.4% of all clinically recognized pregnancies.
295 results
Jump to page
Feedback