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Results by year

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

Year Number of Results
1961 1
1963 1
1967 1
1970 1
1972 1
1973 2
1976 2
1985 3
1987 1
1988 1
1989 1
1990 4
1991 2
1992 2
1993 4
1994 1
1995 1
1996 3
1997 1
1999 1
2023 0

Text availability

Article attribute

Article type

Publication date

PubMed (OMIM) for id: 343663

34 results

Results by year

Filters applied: . Clear all
Page 1
Ectodermal dysplasia.
ROSSELLI D, GULIENETTI R. ROSSELLI D, et al. Br J Plast Surg. 1961 Oct;14:190-204. doi: 10.1016/s0007-1226(61)80036-2. Br J Plast Surg. 1961. PMID: 14494246 No abstract available.
Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome.
Celli J, Duijf P, Hamel BC, Bamshad M, Kramer B, Smits AP, Newbury-Ecob R, Hennekam RC, Van Buggenhout G, van Haeringen A, Woods CG, van Essen AJ, de Waal R, Vriend G, Haber DA, Yang A, McKeon F, Brunner HG, van Bokhoven H. Celli J, et al. Cell. 1999 Oct 15;99(2):143-53. doi: 10.1016/s0092-8674(00)81646-3. Cell. 1999. PMID: 10535733 Free article.
EEC syndrome and genitourinary anomalies: an update.
Maas SM, de Jong TP, Buss P, Hennekam RC. Maas SM, et al. Am J Med Genet. 1996 Jun 14;63(3):472-8. doi: 10.1002/(SICI)1096-8628(19960614)63:3<472::AID-AJMG11>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8737655 Review.
The EEC syndrome: a literature study.
Roelfsema NM, Cobben JM. Roelfsema NM, et al. Clin Dysmorphol. 1996 Apr;5(2):115-27. doi: 10.1097/00019605-199604000-00003. Clin Dysmorphol. 1996. PMID: 8723561 Review.
34 results