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8. 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]
9. 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]
10. A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting. Pozo G; Canún S; Kofman-Alfaro S; Zenteno JC Br J Dermatol; 2004 Oct; 151(4):930-2. PubMed ID: 15491445 [No Abstract] [Full Text] [Related]
11. Hypohidrotic ectodermal dysplasia and intrathoracic neuroblastoma. Buoni S; Zannolli R; Macucci F; Molinelli M; Viviano M; Cuccia A; Hayek J; Volterrani L; de Santi MM; Miracco C; Fois A Pediatr Dermatol; 2007; 24(3):267-71. PubMed ID: 17542878 [TBL] [Abstract][Full Text] [Related]
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13. [Goltz syndrome (focal dermal hypoplasia): a case report (author's transl)]. Sellitto F; Zeppa M; Scarano G; Pilla LM; Angrisani P; Galluccio A Pediatr Med Chir; 1981; 3(6):563-6. PubMed ID: 6806785 [No Abstract] [Full Text] [Related]
14. Adams Oliver syndrome--a variant. Anandan V; Parveen B; Prabhavathy D; Priyavarthini V Int J Dermatol; 2008 Dec; 47(12):1260-2. PubMed ID: 19126012 [No Abstract] [Full Text] [Related]
16. [Ectodermal dysplasia: a heterogenic deviation]. Merkx MA; Arnold WP Ned Tijdschr Tandheelkd; 1995 Sep; 102(9):334-6. PubMed ID: 11837100 [TBL] [Abstract][Full Text] [Related]
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