203 related articles for article (PubMed ID: 23662261)
1. Gene p63: In ectrodactyly-ectodermal dysplasia clefting, ankyloblepharon-ectodermal dysplasia, Rapp-Hodgkin syndrome.
van Straten C; Butow KW
Ann Maxillofac Surg; 2013 Jan; 3(1):58-61. PubMed ID: 23662261
[TBL] [Abstract][Full Text] [Related]
2. Ocular Manifestations in Patients Affected by p63-Associated Disorders: Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) and Ankyloblepharon-Ectodermal Defects-Cleft Lip Palate (AEC) Syndromes.
Di Iorio E; Bonelli F; Bievel-Radulescu R; Decastello N; Ferrari S; Barbaro V; Ponzin D
J Clin Med; 2023 Nov; 12(23):. PubMed ID: 38068429
[TBL] [Abstract][Full Text] [Related]
3. Ectodermal dysplasias associated with clefting: significance of scalp dermatitis.
Fosko SW; Stenn KS; Bolognia JL
J Am Acad Dermatol; 1992 Aug; 27(2 Pt 1):249-56. PubMed ID: 1341424
[TBL] [Abstract][Full Text] [Related]
4. Ectodermal dysplasias: the p63 tail.
Tadini G; Santagada F; Brena M; Pezzani L; Nannini P
G Ital Dermatol Venereol; 2013 Feb; 148(1):53-8. PubMed ID: 23407076
[TBL] [Abstract][Full Text] [Related]
5. A newborn with overlapping features of AEC and EEC syndromes.
Celik TH; Buyukcam A; Simsek-Kiper PO; Utine GE; Ersoy-Evans S; Korkmaz A; Yntema HG; Bodugroglu K; Yurdakok M
Am J Med Genet A; 2011 Dec; 155A(12):3100-3. PubMed ID: 22065614
[TBL] [Abstract][Full Text] [Related]
6. Mixed clefting type in Rapp-Hodgkin syndrome.
Neilson DE; Brunger JW; Heeger S; Bamshad M; Robin NH
Am J Med Genet; 2002 Apr; 108(4):281-4. PubMed ID: 11920831
[TBL] [Abstract][Full Text] [Related]
7. Cleft lip and palate repair in Hay-Wells/ankyloblepharon-ectodermal dysplasia-clefting syndrome.
Cabiling DS; Yan AC; McDonald-McGinn DM; Zackai EH; Kirschner RE
Cleft Palate Craniofac J; 2007 May; 44(3):335-9. PubMed ID: 17477760
[TBL] [Abstract][Full Text] [Related]
8. Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up.
Serra G; Antona V; Giuffré M; Li Pomi F; Lo Scalzo L; Piro E; Schierz IAM; Corsello G
Ital J Pediatr; 2021 Sep; 47(1):196. PubMed ID: 34583755
[TBL] [Abstract][Full Text] [Related]
9. A spectrum of TP63-related disorders with eight affected individuals in five unrelated families.
Soğukpınar M; Utine GE; Boduroğlu K; Şimşek-Kiper PÖ
Eur J Med Genet; 2024 Apr; 68():104911. PubMed ID: 38281558
[TBL] [Abstract][Full Text] [Related]
10. Sweating ability of patients with p63-associated syndromes.
Ferstl P; Wohlfart S; Schneider H
Eur J Pediatr; 2018 Nov; 177(11):1727-1731. PubMed ID: 30088137
[TBL] [Abstract][Full Text] [Related]
11. Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (AEC).
Rinne T; Bolat E; Meijer R; Scheffer H; van Bokhoven H
Am J Med Genet A; 2009 Sep; 149A(9):1948-51. PubMed ID: 19676060
[TBL] [Abstract][Full Text] [Related]
12. Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
McGrath JA; Duijf PH; Doetsch V; Irvine AD; de Waal R; Vanmolkot KR; Wessagowit V; Kelly A; Atherton DJ; Griffiths WA; Orlow SJ; van Haeringen A; Ausems MG; Yang A; McKeon F; Bamshad MA; Brunner HG; Hamel BC; van Bokhoven H
Hum Mol Genet; 2001 Feb; 10(3):221-9. PubMed ID: 11159940
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia.
Kantaputra PN; Hamada T; Kumchai T; McGrath JA
J Dent Res; 2003 Jun; 82(6):433-7. PubMed ID: 12766194
[TBL] [Abstract][Full Text] [Related]
17. [Pili torti et canaliculi in ectodermal dysplasia].
Trüeb RM; Spycher MA; Schumacher F; Burg G
Hautarzt; 1994 Jun; 45(6):372-7. PubMed ID: 8071068
[TBL] [Abstract][Full Text] [Related]
18. Rapp-Hodgkin syndrome and AEC syndrome: are they the same entity?
Cambiaghi S; Tadini G; Barbareschi M; Menni S; Caputo R
Br J Dermatol; 1994 Jan; 130(1):97-101. PubMed ID: 8305327
[TBL] [Abstract][Full Text] [Related]
19. Ectodermal dysplasia showing clinical overlap between AEC, Rapp-Hodgkin and CHAND syndromes.
Sahin MT; Türel-Ermertcan A; Chan I; McGrath JA; Oztürkcan S
Clin Exp Dermatol; 2004 Sep; 29(5):486-8. PubMed ID: 15347331
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
