Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

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
1970 1
1971 1
1973 1
1975 1
1976 2
1977 2
1978 1
1979 2
1980 1
1981 1
1982 6
1983 2
1984 2
1985 1
1986 7
1989 1
1990 1
1992 1
1993 1
1995 2
1996 1
1997 2
1998 1
1999 2
2000 1
2001 1
2002 3
2003 3
2005 1
2007 1
2008 5
2009 4
2010 8
2011 5
2013 4
2014 3
2015 1
2016 4
2017 5
2018 4
2019 3
2020 4
2021 3
2022 2
Text availability
Article attribute
Article type
Publication date

Search Results

99 results
Results by year
Filters applied: . Clear all
Page 1
Genetic variants in the KDM6B gene are associated with neurodevelopmental delays and dysmorphic features.
Stolerman ES, Francisco E, Stallworth JL, Jones JR, Monaghan KG, Keller-Ramey J, Person R, Wentzensen IM, McWalter K, Keren B, Heron B, Nava C, Heron D, Kim K, Burton B, Al-Musafri F, O'Grady L, Sahai I, Escobar LF, Meuwissen M, Reyniers E, Kooy F, Lacassie Y, Gunay-Aygun M, Schatz KS, Hochstenbach R, Zwijnenburg PJG, Waisfisz Q, van Slegtenhorst M, Mancini GMS, Louie RJ. Stolerman ES, et al. Among authors: lacassie y. Am J Med Genet A. 2019 Jul;179(7):1276-1286. doi: 10.1002/ajmg.a.61173. Epub 2019 May 23. Am J Med Genet A. 2019. PMID: 31124279
[Trisomy 22].
Raimann E, Alliende MA, Carvajal MV, Belmar MA, Urzúa E, Lacassie Y. Raimann E, et al. Among authors: lacassie y. Rev Chil Pediatr. 1986 Mar-Apr;57(2):164-70. Rev Chil Pediatr. 1986. PMID: 3562951 Spanish. No abstract available.
Further delineation of DDX3X syndrome.
Chanes NM, Wong J, Lacassie Y. Chanes NM, et al. Among authors: lacassie y. Clin Dysmorphol. 2019 Jul;28(3):151-153. doi: 10.1097/MCD.0000000000000263. Clin Dysmorphol. 2019. PMID: 30817323 No abstract available.
Ring 2 chromosome: ten-year follow-up report.
Lacassie Y, Arriaza MI, Vargas A, La Motta I. Lacassie Y, et al. Am J Med Genet. 1999 Jul 16;85(2):117-22. doi: 10.1002/(sici)1096-8628(19990716)85:2<117::aid-ajmg4>3.0.co;2-o. Am J Med Genet. 1999. PMID: 10406663 Review.
Schaaf-Yang syndrome overview: Report of 78 individuals.
McCarthy J, Lupo PJ, Kovar E, Rech M, Bostwick B, Scott D, Kraft K, Roscioli T, Charrow J, Schrier Vergano SA, Lose E, Smiegel R, Lacassie Y, Schaaf CP. McCarthy J, et al. Among authors: lacassie y. Am J Med Genet A. 2018 Dec;176(12):2564-2574. doi: 10.1002/ajmg.a.40650. Epub 2018 Oct 10. Am J Med Genet A. 2018. PMID: 30302899 Free PMC article.
New ocular finding in Baraitser-Winter syndrome (BWS).
Rall N, Leon A, Gomez R, Daroca J, Lacassie Y. Rall N, et al. Among authors: lacassie y. Eur J Med Genet. 2018 Jan;61(1):21-23. doi: 10.1016/j.ejmg.2017.10.006. Epub 2017 Oct 9. Eur J Med Genet. 2018. PMID: 29024830
99 results