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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 6
2013 11
2014 7
2015 5
2016 5
2017 5
2018 11
2019 8
2020 9
2021 5
2022 2
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304 results
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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.
Prenatal ultrasound revealed fetal median facial cleft, oligohydramnios and IUGR. 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
Prenatal ultrasound revealed fetal median facial cleft, oligohydramnios and IUGR. Repeat amniocentesis at 22 weeks of gestation using …
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
[Trisomy 22].
Raimann E, Alliende MA, Carvajal MV, Belmar MA, Urzúa E, Lacassie Y. Raimann E, et al. Rev Chil Pediatr. 1986 Mar-Apr;57(2):164-70. Rev Chil Pediatr. 1986. PMID: 3562951 Spanish. No abstract available.
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.
While the majority of patients with mosaic trisomy 22 had abnormal cognitive development, normal development has also been documented. It is conceivable that children with trisomy 22 mosaicism, with minimal physical findings and normal development are …
While the majority of patients with mosaic trisomy 22 had abnormal cognitive development, normal development has also been doc …
Trisomy 22 mosaicism.
Mollica F, Sorge G, Pavone L. Mollica F, et al. J Med Genet. 1977 Jun;14(3):224-5. doi: 10.1136/jmg.14.3.224. J Med Genet. 1977. PMID: 881717 Free PMC article.
A child with many symptoms of trisomy 22 syndrome is described. The child showed a 46,XY/47,XY,+22 chromosome constitution. This is the first reported case of a trisome 22 phenotype with such a mosaic karyotype....
A child with many symptoms of trisomy 22 syndrome is described. The child showed a 46,XY/47,XY,+22 chromosome constitut …
Trisomy 22 and facioauriculovertebral (Goldenhar) sequence.
Kobrynski L, Chitayat D, Zahed L, McGregor D, Rochon L, Brownstein S, Vekemans M, Albert DL. Kobrynski L, et al. Am J Med Genet. 1993 Apr 1;46(1):68-71. doi: 10.1002/ajmg.1320460111. Am J Med Genet. 1993. PMID: 8494034 Review.
We report on an infant girl born with complete trisomy 22 and left hemifacial microsomia, ear anomaly, and limbal and epibulbar complex choristoma. Trisomy 22 was confirmed by prometaphase chromosome analysis and in situ hybridization. ...
We report on an infant girl born with complete trisomy 22 and left hemifacial microsomia, ear anomaly, and limbal and epibulba …
Clinical and molecular studies in full trisomy 22: further delineation of the phenotype and review of the literature.
Bacino CA, Schreck R, Fischel-Ghodsian N, Pepkowitz S, Prezant TR, Graham JM Jr. Bacino CA, et al. Am J Med Genet. 1995 May 8;56(4):359-65. doi: 10.1002/ajmg.1320560404. Am J Med Genet. 1995. PMID: 7604844 Review.
Trisomy 22 is commonly found among spontaneous abortions, second in frequency of occurrence only to trisomy 16. ...Parental origin of the extra chromosome does not seem to play a role in late survival for trisomy 22....
Trisomy 22 is commonly found among spontaneous abortions, second in frequency of occurrence only to trisomy 16. ...Pare
Tertiary trisomy (22q11q),47,+der(22),t(11;22).
Biederman BM, Lin CC, Lowry RB, Somerville R. Biederman BM, et al. Hum Genet. 1980 Feb;53(2):173-7. doi: 10.1007/BF00273491. Hum Genet. 1980. PMID: 7358384
We describe a case of tertiary trisomy (22q11q) 47,XX,+der(22),(22pter = to 22q13 :: 11q25 = to 11qter) in a child with mental retardation, cleft palate, and congenital heart disease resulting from 3 : 1 meiotic nondisjunction in a maternal (11;22) translocat …
We describe a case of tertiary trisomy (22q11q) 47,XX,+der(22),(22pter = to 22q13 :: 11q25 = to 11qter) in a child with mental …
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
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 …
304 results