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5. A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23. Lee YA; Stevens HP; Delaporte E; Wahn U; Reis A Am J Hum Genet; 2000 Jan; 66(1):326-30. PubMed ID: 10631162 [No Abstract] [Full Text] [Related]
6. Evidence for clinical and genetic heterogeneity in hereditary benign telangiectasia. Molho-Pessach V; Agha Z; Libster D; Lerer I; Burger A; Jaber S; Abeliovich D; Zlotogorski A J Am Acad Dermatol; 2007 Nov; 57(5):814-8. PubMed ID: 17658662 [TBL] [Abstract][Full Text] [Related]
7. Huriez syndrome with squamous cell carcinoma. Man XY; Li W; Chen JQ; Zhou J; Liao YJ; Li CM; Cai SQ; Zheng M Eur J Dermatol; 2011; 21(2):294-5. PubMed ID: 21382785 [No Abstract] [Full Text] [Related]
8. Claude Huriez and his syndrome. Al Aboud K; Khachemoune A Skinmed; 2011; 9(5):313-4. PubMed ID: 22165047 [TBL] [Abstract][Full Text] [Related]
9. [Follicular atrophoderma, basal cell proliferation and hypotrichosis (Bazex-Dupré-Christol syndrome). A study in 2 families]. Moreau-Cabarrot A; Bonafé JL; Hachich N; Jalby BC; Aubert G; Rolland M; Bazex J Ann Dermatol Venereol; 1994; 121(4):297-301. PubMed ID: 7702247 [TBL] [Abstract][Full Text] [Related]
10. Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree. Richards JE; Ritch R; Lichter PR; Rozsa FW; Stringham HM; Caronia RM; Johnson D; Abundo GP; Willcockson J; Downs CA; Thompson DA; Musarella MA; Gupta N; Othman MI; Torrez DM; Herman SB; Wong DJ; Higashi M; Boehnke M Ophthalmology; 1998 Sep; 105(9):1698-707. PubMed ID: 9754180 [TBL] [Abstract][Full Text] [Related]
12. [Squamous cell carcinoma in Huriez syndrome]. Tadlaoui I; Qasmi S; Belgnaoui F; Bouhllab J; Afifi Y; Meziane M; Senouci K; Hassam B; Zouaidia F; El Khannoussi B; Mahassini N Ann Dermatol Venereol; 2008 Mar; 135(3):249-50. PubMed ID: 18374867 [No Abstract] [Full Text] [Related]
13. Kindler syndrome: report of three cases in a family and a brief review. Yazdanfar A; Hashemi B Int J Dermatol; 2009 Feb; 48(2):145-9. PubMed ID: 19200189 [TBL] [Abstract][Full Text] [Related]
14. Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31. Lagier-Tourenne C; Tranebaerg L; Chaigne D; Gribaa M; Dollfus H; Silvestri G; Bétard C; Warter JM; Koenig M Eur J Hum Genet; 2003 Oct; 11(10):770-8. PubMed ID: 14512967 [TBL] [Abstract][Full Text] [Related]
15. Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome. Loh AYT; Špoljar S; Neo GYW; Escande-Beillard N; Leushacke M; Luijten MNH; Venkatesh B; Bonnard C; van Steensel MAM; Hamm H; Carmichael A; Rajan N; Carney TJ; Reversade B Am J Med Genet A; 2022 Jun; 188(6):1752-1760. PubMed ID: 35212137 [TBL] [Abstract][Full Text] [Related]
17. [Progressive scleroderma of the acrosclerosis type in mother and daughter with multiple skin tumors in the mother]. Meinhof W Z Hautkr; 1974 Aug; 49(15):653-60. PubMed ID: 4428824 [No Abstract] [Full Text] [Related]
18. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3. Tariq M; Chishti MS; Ali G; Ahmad W Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143 [TBL] [Abstract][Full Text] [Related]
19. Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family. Legius E; Schollen E; Matthijs G; Fryns JP Eur J Hum Genet; 1998 Jan; 6(1):32-7. PubMed ID: 9781012 [TBL] [Abstract][Full Text] [Related]
20. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci? Lohmann-Hedrich K; Neumann A; Kleensang A; Lohnau T; Muhle H; Djarmati A; König IR; Pramstaller PP; Schwinger E; Kramer PL; Ziegler A; Stephani U; Klein C Neurology; 2008 Feb; 70(9):686-94. PubMed ID: 18032746 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]