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Year Number of Results
1977 1
1981 1
1986 1
1992 1
1995 2
1996 1
1997 1
1998 1
1999 1
2001 5
2003 1
2004 3
2005 1
2006 1
2007 2
2009 1
2010 2
2012 1
2013 4
2014 2
2016 1
2018 3
2019 2
2020 0
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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.
OBJECTIVE: We present prenatal diagnosis of mosaic trisomy 22 at amniocentesis in a pregnancy with facial cleft, oligohydramnios and intrauterine growth restriction (IUGR), and we review the literature. ...Repeat amniocentesis at 22 weeks of gestation …
OBJECTIVE: We present prenatal diagnosis of mosaic trisomy 22 at amniocentesis in a pregnancy with facial cleft, oligoh …
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 …
BACKGROUND: Trisomy 22 mosaicism is a rare autosomal anomaly with survival compatibility. Recognition of the complete triso
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
While the complete form of trisomy 22 is seemingly incompatible with life, the mosaic form is a rare syndrome associated with developmental delays, intellectual disability, and dysmorphic features. ...Diagnoses such as mosaic trisomy 22 s …
While the complete form of trisomy 22 is seemingly incompatible with life, the mosaic form is a rare syndrome associate …
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. ...While the majority of patients with mosaic trisomy 22 had abnormal cognitive development, normal development h …
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. ...DIAGNOSES: The fetus was diagnosed as having complete non-mosaic trisomy 22 by chromosomal analys …
INTRODUCTION: Complete non-mosaic trisomy 22 is a fatal chromosomal disorder that only few fetuses can survive over 12 …
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. ...Clinical features of liveborn children with non-
Trisomy 22 is the third most common autosomal trisomy occurring in about 0.4% of all clinically recognized pregnancies.
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 tris
Trisomy 22 is a common trisomy in spontaneous abortions. In contrast, live-born trisomy 22 is rarely seen
Mosaic trisomy 22 associated with total colonic aganglionosis and malrotation.
Hall T, Samuel M, Brain J. Hall T, et al. J Pediatr Surg. 2009 Jan;44(1):e9-e11. doi: 10.1016/j.jpedsurg.2008.09.032. J Pediatr Surg. 2009. PMID: 19159711
AIMS: Abnormalities of chromosome 22 karyotype have been reported to be associated with both malrotation and aganglionosis. However, although malrotation has been reported to occur in the rare mosaic trisomy 22, Hirschsprung's disease has not. ...The a …
AIMS: Abnormalities of chromosome 22 karyotype have been reported to be associated with both malrotation and aganglionosis. However, …
Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes.
Crowe CA, Schwartz S, Black CJ, Jaswaney V. Crowe CA, et al. Am J Med Genet. 1997 Sep 5;71(4):406-13. Am J Med Genet. 1997. PMID: 9286446 Review.
In a case of mosaic trisomy 22 the trisomic cells were detected primarily in fibroblasts. Results of initial lymphocyte chromosome analysis were normal. ...The phenotype of this condition overlaps that of non-mosaic trisomy 22 chromosome …
In a case of mosaic trisomy 22 the trisomic cells were detected primarily in fibroblasts. Results of initial lymphocyte …
Two trisomy 22 live births in one hospital in 15 months: is it as rare as we thought?
Naicker T, Aldous C. Naicker T, et al. Fetal Pediatr Pathol. 2014 Feb;33(1):35-41. doi: 10.3109/15513815.2013.842273. Epub 2013 Oct 4. Fetal Pediatr Pathol. 2014. PMID: 24093507
We report two cases of complete non-mosaic trisomy 22 who were born within 15 months of each other in KwaZulu Natal, South Africa. ...We further compare the clinical phenotype of trisomy 22 with those of trisomies 13 and 18 to delineate a clinic …
We report two cases of complete non-mosaic trisomy 22 who were born within 15 months of each other in KwaZulu Natal, So …
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