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

Year Number of Results
1970 3
1971 2
1972 3
1973 2
1974 3
1975 4
1976 2
1977 4
1980 1
1981 2
1984 4
1985 5
1986 5
1987 5
1988 2
1989 3
1990 1
1991 3
1992 7
1993 1
1994 8
1995 6
1996 3
1997 2
1998 4
1999 4
2000 3
2001 11
2002 6
2003 4
2004 4
2005 7
2006 8
2007 8
2008 4
2009 2
2010 6
2011 2
2012 8
2013 10
2014 6
2015 7
2016 5
2017 9
2018 9
2019 14
2020 10
2021 14
2022 7
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236 results
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Page 1
Cat eye syndrome.
Sharma D, Murki S, Pratap T, Vasikarla M. Sharma D, et al. BMJ Case Rep. 2014 May 19;2014:bcr2014203923. doi: 10.1136/bcr-2014-203923. BMJ Case Rep. 2014. PMID: 24842361 Free PMC article.
Karyotyping showed an extra small marker chromosome suggestive of the Cat eye syndrome....
Karyotyping showed an extra small marker chromosome suggestive of the Cat eye syndrome....
[Cat eye syndrome].
Kimura J. Kimura J. Ryoikibetsu Shokogun Shirizu. 2001;(33):339-40. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462464 Review. Japanese. No abstract available.
[Cat eye syndrome].
Bremond-Gignac D, Morin G, Jedraszak G, Receveur A, Rochette J, Copin H. Bremond-Gignac D, et al. J Fr Ophtalmol. 2015 Apr;38(4):368-9. doi: 10.1016/j.jfo.2014.09.016. Epub 2015 Mar 20. J Fr Ophtalmol. 2015. PMID: 25799388 French. No abstract available.
[Cat eye syndrome].
Teraoka M, Narahara K. Teraoka M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):348-9. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057256 Review. Japanese. No abstract available.
[Cat-eye syndrome (a psychiatric aspect)].
Makarov IA, Gavrilina SB, Belozerov BG. Makarov IA, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2019;119(11):60-64. doi: 10.17116/jnevro201911911160. Zh Nevrol Psikhiatr Im S S Korsakova. 2019. PMID: 31851174 Russian.
Cat-eye syndrome is associated with abnormalities in chromosome 22. ...
Cat-eye syndrome is associated with abnormalities in chromosome 22. ...
Cat eye syndrome and growth hormone deficiency with pituitary anomalies: a case report and review of the literature.
Melo C, Gama-de-Sousa S, Almeida F, Rendeiro P, Tavares P, Cardoso H, Carvalho S. Melo C, et al. Gene. 2013 Oct 15;529(1):186-9. doi: 10.1016/j.gene.2013.07.031. Epub 2013 Aug 6. Gene. 2013. PMID: 23928108 Review.
We report a girl with cat eye syndrome, presenting short stature, with growth hormone deficiency due to posterior pituitary ectopia. ...A review on short stature and growth hormone deficiency in cat eye syndrome is conducted....
We report a girl with cat eye syndrome, presenting short stature, with growth hormone deficiency due to posterior pitui …
Mosaic cat eye syndrome in a child with unilateral iris coloboma.
Hernández-Medrano C, Hidalgo-Bravo A, Villanueva-Mendoza C, Bautista-Tirado T, Apam-Garduño D. Hernández-Medrano C, et al. Ophthalmic Genet. 2021 Feb;42(1):84-87. doi: 10.1080/13816810.2020.1839918. Epub 2020 Dec 1. Ophthalmic Genet. 2021. PMID: 33465332
BACKGROUND: Cat eye syndrome (CES) is a rare chromosomal disorder with a known incidence of 1 per 50,000-150,000 live newborns. ...The aim of this report is to present a patient with unilateral iris coloboma related to a mosaicism of cat eye
BACKGROUND: Cat eye syndrome (CES) is a rare chromosomal disorder with a known incidence of 1 per 50,000-150,000 live n …
[Cat-eye syndrome. Clinical and cytogenetical differentialdiagnosis (author's transl)].
Kunze J, Tolksdorf M, Wiedemann HR. Kunze J, et al. Humangenetik. 1975;26(4):271-89. Humangenetik. 1975. PMID: 50268 Review. German.
We report a 5 1/2-year-old girl whose clinical symptoms are consistent with diagnosis of the cat-eye syndrome. The prominent symptoms are: anal stenosis, preauricular tags and pits, coloboma of the iris, doubling of the pelvis and ureter on both sides, vesico …
We report a 5 1/2-year-old girl whose clinical symptoms are consistent with diagnosis of the cat-eye syndrome. The prom …
Müllerian Agenesis in Cat Eye Syndrome and 22q11 Chromosome Abnormalities: A Case Report and Literature Review.
AlSubaihin A, VanderMeulen J, Harris K, Duck J, McCready E. AlSubaihin A, et al. J Pediatr Adolesc Gynecol. 2018 Apr;31(2):158-161. doi: 10.1016/j.jpag.2017.09.004. Epub 2017 Sep 14. J Pediatr Adolesc Gynecol. 2018. PMID: 28919146 Review.
Mullerian agenesis has been reported as a rare finding associated with chromosomal aberrations of the 22q11 chromosomal region including at least 1 individual with cat eye syndrome (CES) and 10 individuals with deletions or duplications of the 22q11.2 region. …
Mullerian agenesis has been reported as a rare finding associated with chromosomal aberrations of the 22q11 chromosomal region including at …
236 results