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42. [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]
43. Osseointegrated implants in the oral rehabilitation of a patient with cleft lip and palate and ectodermal dysplasia: a case report. de Rezende ML; Amado FM Int J Oral Maxillofac Implants; 2004; 19(6):896-900. PubMed ID: 15623068 [TBL] [Abstract][Full Text] [Related]
44. Hay-Wells syndrome in a child with mutation in the TP73L gene. Garcia Bartels N; Neumann LM; Mleczko A; Rubach K; Peters H; Rossi R; Sterry W; Blume-Peytavi U J Dtsch Dermatol Ges; 2007 Oct; 5(10):919-23. PubMed ID: 17910675 [TBL] [Abstract][Full Text] [Related]
45. A new autosomal recessive disorder resembling Weaver syndrome. Teebi AS; Sundareshan TS; Hammouri MY; al-Awadi SA; al-Saleh QA Am J Med Genet; 1989 Aug; 33(4):479-82. PubMed ID: 2596508 [TBL] [Abstract][Full Text] [Related]
50. Hypohidrotic ectodermal dysplasia: dental features and carriers detection. Glavina D; Majstorović M; Lulić-Dukić O; Jurić H Coll Antropol; 2001 Jun; 25(1):303-10. PubMed ID: 11787554 [TBL] [Abstract][Full Text] [Related]
51. Hypohidrotic ectodermal dysplasia: dental, clinical, genetic and dermatoglyphic findings of three cases. Kargül B; Alcan T; Kabalay U; Atasu M J Clin Pediatr Dent; 2001; 26(1):5-12. PubMed ID: 11688814 [TBL] [Abstract][Full Text] [Related]
52. [Anhydrotic ectodermal dysplasia]. Claisse Alamán E; Benavides de Larraza G; Espinosa Morett A Bol Med Hosp Infant Mex; 1976; 33(5):1185-95. PubMed ID: 973866 [TBL] [Abstract][Full Text] [Related]
53. Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene. Rinne T; Spadoni E; Kjaer KW; Danesino C; Larizza D; Kock M; Huoponen K; Savontaus ML; Aaltonen M; Duijf P; Brunner HG; Penttinen M; van Bokhoven H Eur J Hum Genet; 2006 Aug; 14(8):904-10. PubMed ID: 16724007 [TBL] [Abstract][Full Text] [Related]
54. Autosomal recessive ectodermal dysplasia: I. An undescribed dysplasia/malformation syndrome. Bustos T; Simosa V; Pinto-Cisternas J; Abramovits W; Jolay L; Rodriguez L; Fernandez L; Ramela M Am J Med Genet; 1991 Dec; 41(4):398-404. PubMed ID: 1776626 [TBL] [Abstract][Full Text] [Related]
56. 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]
57. 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]
58. Evaluation of ectodermal dysplasia. Baskan Z; Yavuz I; Ulku R; Kaya S; Yavuz Y; Basaran G; Adiguzel O; Ozer T Kaohsiung J Med Sci; 2006 Apr; 22(4):171-6. PubMed ID: 16679298 [TBL] [Abstract][Full Text] [Related]
59. [Anhidrotic ectodermal dysplasia. Clinico-genetic study of 4 families]. Balestrazzi P; Solli R; Salami P; Corrini L; Mattioli M; Bernasconi S Minerva Pediatr; 1979 Feb; 31(4):265-74. PubMed ID: 460084 [No Abstract] [Full Text] [Related]
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