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

Filters

My Custom Filters

Edit custom filters

Results by year

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

Year Number of Results
1945 1
1946 1
1947 2
1948 2
1949 2
1950 3
1951 5
1952 9
1953 10
1954 11
1955 15
1956 12
1957 12
1958 8
1959 16
1960 7
1961 6
1962 11
1963 26
1964 29
1965 20
1966 20
1967 20
1968 25
1969 27
1970 26
1971 35
1972 29
1973 29
1974 22
1975 26
1976 37
1977 40
1978 21
1979 26
1980 28
1981 43
1982 31
1983 32
1984 39
1985 31
1986 41
1987 44
1988 60
1989 43
1990 43
1991 33
1992 51
1993 45
1994 34
1995 32
1996 42
1997 46
1998 54
1999 52
2000 62
2001 76
2002 67
2003 67
2004 73
2005 85
2006 58
2007 50
2008 80
2009 98
2010 69
2011 83
2012 97
2013 112
2014 108
2015 102
2016 84
2017 92
2018 88
2019 79
2020 94
2021 92
2022 82
2023 89
2024 59
2025 70
2026 28

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

3,321 results

Results by year

Filters applied: . Clear all
Page 1
LEF1 haploinsufficiency causes ectodermal dysplasia.
Lévy J, Capri Y, Rachid M, Dupont C, Vermeesch JR, Devriendt K, Verloes A, Tabet AC, Bailleul-Forestier I. Lévy J, et al. Clin Genet. 2020 Apr;97(4):595-600. doi: 10.1111/cge.13714. Epub 2020 Feb 17. Clin Genet. 2020. PMID: 32022899
Prevalence rates for ectodermal dysplasia syndromes.
Butcher C, Abbott BM, Grange D, Fete M, Meyer B, Spinka C, Fete T. Butcher C, et al. Am J Med Genet A. 2024 Dec;194(12):e63832. doi: 10.1002/ajmg.a.63832. Epub 2024 Aug 9. Am J Med Genet A. 2024. PMID: 39126172
Ocular manifestations of ectodermal dysplasia.
Landau Prat D, Katowitz WR, Strong A, Katowitz JA. Landau Prat D, et al. Orphanet J Rare Dis. 2021 May 1;16(1):197. doi: 10.1186/s13023-021-01824-2. Orphanet J Rare Dis. 2021. PMID: 33933124 Free PMC article.
RASopathies: Dermatologists' viewpoints.
Palit A, Inamadar AC. Palit A, et al. Indian J Dermatol Venereol Leprol. 2022 May-Jun;88(4):452-463. doi: 10.25259/IJDVL_799_20. Indian J Dermatol Venereol Leprol. 2022. PMID: 35138057 Free article. Review.
The fundamentals of WNT10A.
Benard EL, Hammerschmidt M. Benard EL, et al. Differentiation. 2025 Mar-Apr;142:100838. doi: 10.1016/j.diff.2025.100838. Epub 2025 Jan 30. Differentiation. 2025. PMID: 39904689 Free PMC article. Review.
Clouston Syndrome.
Ahmed C, Trope BM, Amorim G, Ribeiro M, Ramos-E-Silva M. Ahmed C, et al. Skinmed. 2021 Feb 1;19(1):54. eCollection 2021. Skinmed. 2021. PMID: 33658115 No abstract available.
p63 in corneal and epidermal differentiation.
Novelli F, Ganini C, Melino G, Nucci C, Han Y, Shi Y, Wang Y, Candi E. Novelli F, et al. Biochem Biophys Res Commun. 2022 Jun 25;610:15-22. doi: 10.1016/j.bbrc.2022.04.022. Epub 2022 Apr 9. Biochem Biophys Res Commun. 2022. PMID: 35430447 Review.
3,321 results