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1962
2025

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

Year Number of Results
1962 2
1963 92
1964 151
1965 99
1966 115
1967 160
1968 217
1969 178
1970 218
1971 271
1972 293
1973 308
1974 295
1975 255
1976 236
1977 208
1978 275
1979 282
1980 274
1981 376
1982 297
1983 333
1984 350
1985 381
1986 421
1987 591
1988 966
1989 981
1990 1075
1991 1183
1992 1308
1993 1464
1994 1344
1995 1473
1996 1595
1997 1502
1998 1560
1999 1586
2000 1893
2001 2006
2002 1606
2003 1604
2004 1886
2005 1957
2006 2009
2007 1969
2008 1998
2009 1950
2010 2201
2011 2287
2012 2505
2013 2529
2014 2690
2015 2639
2016 2722
2017 2806
2018 2736
2019 2798
2020 2833
2021 2829
2022 2854
2023 2631
2024 2409
2025 152

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74,769 results

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Page 1
The RASopathies.
Rauen KA. Rauen KA. Annu Rev Genomics Hum Genet. 2013;14:355-69. doi: 10.1146/annurev-genom-091212-153523. Epub 2013 Jul 15. Annu Rev Genomics Hum Genet. 2013. PMID: 23875798 Free PMC article. Review.
Ebstein's Anomaly: From Fetus to Adult-Literature Review and Pathway for Patient Care.
Ramcharan TKW, Goff DA, Greenleaf CE, Shebani SO, Salazar JD, Corno AF. Ramcharan TKW, et al. Pediatr Cardiol. 2022 Oct;43(7):1409-1428. doi: 10.1007/s00246-022-02908-x. Epub 2022 Apr 23. Pediatr Cardiol. 2022. PMID: 35460366 Review.
Ebstein's anomaly, first described in 1866 by Dr William Ebstein, accounts for 0.3-0.5% of congenital heart defects and represents 40% of congenital tricuspid valve abnormalities. ...This article summarizes and analyzes the literature on Ebstein's a
Ebstein's anomaly, first described in 1866 by Dr William Ebstein, accounts for 0.3-0.5% of congenital heart defects and repres …
Congenital malformations.
Corsello G, Giuffrè M. Corsello G, et al. J Matern Fetal Neonatal Med. 2012 Apr;25 Suppl 1:25-9. doi: 10.3109/14767058.2012.664943. Epub 2012 Mar 14. J Matern Fetal Neonatal Med. 2012. PMID: 22356564 Free article. Review.
Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or during the intrauterine life. ...Both genetic and environmental factors, as well as their combination in a multifactorial contest, may induce
Congenital malformations are single or multiple defects of the morphogenesis of organs or body districts identifiable at birth or dur
The prevalence of congenital anomalies in Europe.
Dolk H, Loane M, Garne E. Dolk H, et al. Adv Exp Med Biol. 2010;686:349-64. doi: 10.1007/978-90-481-9485-8_20. Adv Exp Med Biol. 2010. PMID: 20824455 Review.
EUROCAT (European Surveillance of Congenital Anomalies) is the network of population-based registers of congenital anomaly in Europe, with a common protocol and data quality review, covering 1.5 million annual births in 22 countries. EUROCAT recorded a total …
EUROCAT (European Surveillance of Congenital Anomalies) is the network of population-based registers of congenital anomaly
Systematic review of first-trimester ultrasound screening for detection of fetal structural anomalies and factors that affect screening performance.
Karim JN, Roberts NW, Salomon LJ, Papageorghiou AT. Karim JN, et al. Ultrasound Obstet Gynecol. 2017 Oct;50(4):429-441. doi: 10.1002/uog.17246. Epub 2017 Sep 7. Ultrasound Obstet Gynecol. 2017. PMID: 27546497 Free article. Review.
OBJECTIVES: To determine the sensitivity and specificity of first-trimester ultrasound for the detection of fetal abnormalities and to establish which factors might impact on screening performance. METHODS: A systematic review and meta-analysis of all relevant publi …
OBJECTIVES: To determine the sensitivity and specificity of first-trimester ultrasound for the detection of fetal abnormalities
Diversity and dysmorphology.
Kruszka P, Tekendo-Ngongang C, Muenke M. Kruszka P, et al. Curr Opin Pediatr. 2019 Dec;31(6):702-707. doi: 10.1097/MOP.0000000000000816. Curr Opin Pediatr. 2019. PMID: 31693576 Review.
Recognizing patterns of dysmorphic features is a critical step in the diagnosis and management of human congenital anomalies and genetic syndromes. This review presents recent developments in genetic syndromes and their related dysmorphology in diverse populations. ...
Recognizing patterns of dysmorphic features is a critical step in the diagnosis and management of human congenital anomalies and gene …
Perinatal hospice.
Hoeldtke NJ, Calhoun BC. Hoeldtke NJ, et al. Am J Obstet Gynecol. 2001 Sep;185(3):525-9. doi: 10.1067/mob.2001.116093. Am J Obstet Gynecol. 2001. PMID: 11568772 Review.
When the prenatal diagnosis of a lethal fetal anomaly has been established, some patients choose to continue their pregnancy. ...
When the prenatal diagnosis of a lethal fetal anomaly has been established, some patients choose to continue their pregnancy. …
Airway Anomalies.
Landry AM, Rutter MJ. Landry AM, et al. Clin Perinatol. 2018 Dec;45(4):597-607. doi: 10.1016/j.clp.2018.07.002. Epub 2018 Sep 11. Clin Perinatol. 2018. PMID: 30396407 Review.
This article reviews congenital anomalies involving the larynx and trachea, including congenital subglottic stenosis, laryngeal webs, laryngeal cleft, and tracheal stenosis. ...
This article reviews congenital anomalies involving the larynx and trachea, including congenital subglottic stenosis, laryngea …
Fetal akinesia.
Hammond E, Donnenfeld AE. Hammond E, et al. Obstet Gynecol Surv. 1995 Mar;50(3):240-9. doi: 10.1097/00006254-199503000-00028. Obstet Gynecol Surv. 1995. PMID: 7739837 Review.
Normal fetal growth and development during pregnancy is highly dependent upon adequate fetal movement. Limitation of movement, regardless of the underlying cause, can result in a particular pattern of abnormal fetal morphogenesis. This phenotype is termed the …
Normal fetal growth and development during pregnancy is highly dependent upon adequate fetal movement. Limitation of movement, …
[Mayer-Rokitansky-Küster-Hauser syndrome].
Herlin M, Petersen MB. Herlin M, et al. Ugeskr Laeger. 2017 Mar 27;179(13):V10160744. Ugeskr Laeger. 2017. PMID: 28397650 Free article. Review. Danish.
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital anomaly characterized by uterovaginal agenesis in females with normal secondary sex characteristics and normal karyotype (46,XX). ...
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital anomaly characterized by uterovaginal agenesis in females with …
74,769 results
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