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9. A new autosomal dominant syndrome of hypohidrotic ectodermal dysplasia and unusual facies. Bocian M; Rimoin DL Birth Defects Orig Artic Ser; 1979; 15(5B):239-51. PubMed ID: 526580 [No Abstract] [Full Text] [Related]
10. Family with autosomal dominant hidrotic ectodermal dysplasia: a previously unrecognised syndrome? Christianson AL; Fourie S Am J Med Genet; 1996 Jun; 63(4):549-53. PubMed ID: 8826433 [TBL] [Abstract][Full Text] [Related]
11. [Familial form of ectodermal dysplasia]. Broniewski M; Chilman W; Lisiecka K; Uniecka W Pol Tyg Lek; 1973 Feb; 28(7):256-8. PubMed ID: 4691199 [No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. [Hypohidrotic ectodermal dysplasia syndrome. Description of a clinical case]. Bonvini G; Cotta-Ramusino A; Pagliano-Sassi L Pediatr Med Chir; 1989; 11(4):467-9. PubMed ID: 2694110 [TBL] [Abstract][Full Text] [Related]
15. Three novel mutations of the EDA gene in Chinese patients with X-linked hypohidrotic ectodermal dysplasia. Zhao J; Hua R; Zhao X; Meng Y; Ao Y; Liu Q; Shang D; Sun M; Lo WH; Zhang X Br J Dermatol; 2008 Mar; 158(3):614-7. PubMed ID: 18076698 [No Abstract] [Full Text] [Related]
16. Letter regarding the article: "R298Q mutation of p63 gene in autosomal dominant ectodermal dysplasia associated with arrhythmogenic right ventricular cardiomyopathy" by Valenzise et al. van der Zwaag PA; Jongbloed JD; van den Berg MP; Jonkman MF; van Tintelen JP Eur J Med Genet; 2009; 52(4):277. PubMed ID: 19450441 [No Abstract] [Full Text] [Related]
17. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. Aswegan AL; Josephson KD; Mowbray R; Pauli RM; Spritz RA; Williams MS Am J Med Genet; 1997 Nov; 72(4):462-7. PubMed ID: 9375732 [TBL] [Abstract][Full Text] [Related]
18. Further examples of autosomal dominant transmission of nonsyndromic aplasia cutis congenita. Elliott AM; Teebi AS Am J Med Genet; 1997 Dec; 73(4):495-6. PubMed ID: 9415483 [No Abstract] [Full Text] [Related]
19. Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation: a possible "new" form of ectodermal dysplasia. Winter RM; MacDermot KD; Hill FJ Am J Med Genet; 1988 Jan; 29(1):209-16. PubMed ID: 3344769 [TBL] [Abstract][Full Text] [Related]
20. [Clouston's ectodermal dysplasia. A case report with biochemical study of keratin]. Giraud F; Mattei JF; Rolland M; Ghiglione C; Pommier de Sante P; Sudan N Arch Fr Pediatr; 1977 Dec; 34(10):982-93. PubMed ID: 610663 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]