696 related articles for article (PubMed ID: 19716498)
1. A 19-year follow-up of a patient with type 3 ectrodactyly-ectodermal dysplasia-clefting syndrome who developed non-Hodgkin lymphoma.
Balci S; Engiz O; Okten G; Sipahier M; Gursu G; Kandemir B
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e91-5. PubMed ID: 19716498
[TBL] [Abstract][Full Text] [Related]
2. A novel H208D TP63 mutation in a familial case of ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome without clefting.
Sorasio L; Biamino E; Garelli E; Ferrero GB; Silengo MC
Clin Exp Dermatol; 2009 Dec; 34(8):e726-8. PubMed ID: 19663851
[TBL] [Abstract][Full Text] [Related]
3. Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.
Clements SE; Techanukul T; Coman D; Mellerio JE; McGrath JA
Br J Dermatol; 2010 Jan; 162(1):201-7. PubMed ID: 19903181
[TBL] [Abstract][Full Text] [Related]
4. ADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene.
Chan I; Harper JI; Mellerio JE; McGrath JA
Clin Exp Dermatol; 2004 Nov; 29(6):669-72. PubMed ID: 15550149
[TBL] [Abstract][Full Text] [Related]
5. Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.
Paranaíba LM; Martelli-Júnior H; de Miranda RT; Bufalino A; Abdo Filho RC; Coletta RD
Cleft Palate Craniofac J; 2010 Sep; 47(5):544-7. PubMed ID: 20180707
[TBL] [Abstract][Full Text] [Related]
6. The EEC syndrome and SHFM: report of two cases and mutation analysis of p63 gene.
Ergin H; Semerci CN; Karakuş YT; Scheffer H; Ergin S; Koltuksuz U; Meijer R; Satiroğlu-Tufan NL
Turk J Pediatr; 2010; 52(5):529-33. PubMed ID: 21434540
[TBL] [Abstract][Full Text] [Related]
7. A case of ankyloblepharon, ectodermal dysplasia, and cleft lip/palate syndrome with ectrodactyly: are the p63 syndromes distinct after all?
Chiu YE; Drolet BA; Duffy KJ; Holland KE
Pediatr Dermatol; 2011; 28(1):15-9. PubMed ID: 19793345
[TBL] [Abstract][Full Text] [Related]
8. Ectodermal dysplasia, Rapp-Hodgkin type in a mother and severe ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC) in her child.
Moerman P; Fryns JP
Am J Med Genet; 1996 Jun; 63(3):479-81. PubMed ID: 8737656
[TBL] [Abstract][Full Text] [Related]
9. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome.
Shotelersuk V; Janklat S; Siriwan P; Tongkobpetch S
Clin Exp Dermatol; 2005 May; 30(3):282-5. PubMed ID: 15807690
[TBL] [Abstract][Full Text] [Related]
10. p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly.
Berdón-Zapata V; Granillo-Alvarez M; Valdés-Flores M; García-Ortiz JE; Kofman-Alfaro S; Zenteno JC
J Orthop Res; 2004 Jan; 22(1):1-5. PubMed ID: 14656652
[TBL] [Abstract][Full Text] [Related]
11. Prune belly anomaly on prenatal ultrasound as a presenting feature of ectrodactyly-ectodermal dysplasia-clefting syndrome (EEC).
Janssens S; Defoort P; Vandenbroecke C; Scheffer H; Mortier G
Genet Couns; 2008; 19(4):433-7. PubMed ID: 19239089
[TBL] [Abstract][Full Text] [Related]
12. Ankyloblepharon-ectodermal dysplasia-clefting syndrome: a novel p63 mutation associated with generalized neonatal erosions.
Sawardekar SS; Zaenglein AL
Pediatr Dermatol; 2011; 28(3):313-7. PubMed ID: 20738799
[TBL] [Abstract][Full Text] [Related]
13. p63-associated disorders.
Rinne T; Brunner HG; van Bokhoven H
Cell Cycle; 2007 Feb; 6(3):262-8. PubMed ID: 17224651
[TBL] [Abstract][Full Text] [Related]
14. R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy.
Valenzise M; Arrigo T; De Luca F; Privitera A; Frigiola A; Carando A; Garelli E; Silengo M
Eur J Med Genet; 2008; 51(5):497-500. PubMed ID: 18603493
[TBL] [Abstract][Full Text] [Related]
15. An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology.
Prontera P; Escande F; Cocchi G; Donti E; Martini A; Sensi A
Genet Couns; 2008; 19(4):397-402. PubMed ID: 19239083
[TBL] [Abstract][Full Text] [Related]
16. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate (EEC) syndrome without clefting: a rare case report.
Malvankar DD; Sacchidanand S; Mallikarjun M
Dermatol Online J; 2012 Feb; 18(2):5. PubMed ID: 22398226
[TBL] [Abstract][Full Text] [Related]
17. Counseling dilemmas in EEC syndrome.
Tekin M; Ohle C; Johnson DE; Christmas JT; Bodurtha J
Genet Couns; 2000; 11(1):19-24. PubMed ID: 10756423
[TBL] [Abstract][Full Text] [Related]
18. ADULT syndrome caused by a mutation previously associated with EEC syndrome.
Avitan-Hersh E; Indelman M; Bergman R; Sprecher E
Pediatr Dermatol; 2010; 27(6):643-5. PubMed ID: 21078104
[TBL] [Abstract][Full Text] [Related]
19. EEC syndrome (ectrodactyly-ectodermal dysplasia-clefting): a clinical case report.
Ulukapi I; Bilgin T; Yalçin S
ASDC J Dent Child; 2001; 68(5-6):350-2, 302. PubMed ID: 11985198
[TBL] [Abstract][Full Text] [Related]
20. Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous-Heterozygous Mosaicism of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome.
Barbaro V; Nasti AA; Raffa P; Migliorati A; Nespeca P; Ferrari S; Palumbo E; Bertolin M; Breda C; Miceli F; Russo A; Caenazzo L; Ponzin D; Palù G; Parolin C; Di Iorio E
Stem Cells Transl Med; 2016 Aug; 5(8):1098-105. PubMed ID: 27151912
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
