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9. Homozygosity mapping of a Weill-Marchesani syndrome locus to chromosome 19p13.3-p13.2. Faivre L; Mégarbané A; Alswaid A; Zylberberg L; Aldohayan N; Campos-Xavier B; Bacq D; Legeai-Mallet L; Bonaventure J; Munnich A; Cormier-Daire V Hum Genet; 2002 Apr; 110(4):366-70. PubMed ID: 11941487 [TBL] [Abstract][Full Text] [Related]
10. Weill-Marchesani syndrome in mother and son. Young ID; Fielder AR; Casey TA Clin Genet; 1986 Dec; 30(6):475-80. PubMed ID: 3493095 [TBL] [Abstract][Full Text] [Related]
11. Sclerosis of the skin in the GEMSS syndrome. An overproduction of normal collagen. Kunz M; Paulus W; Sollberg S; Weilbach F; Voeske W; Ludwig G; Bröcker EB; Hamm H Arch Dermatol; 1995 Oct; 131(10):1170-4. PubMed ID: 7574834 [TBL] [Abstract][Full Text] [Related]
12. [Lens coloboma and lens dislocation in Stickler (Marshall) syndrome]. Schlote T; Völker M; Knorr M; Thiel HJ Klin Monbl Augenheilkd; 1997 Apr; 210(4):227-8. PubMed ID: 9235398 [TBL] [Abstract][Full Text] [Related]
16. [Weill Marchesani syndrome. Report of a case]. el Kettani A; Hamdani M; Rais L; el Belhadji M; Rachid R; Laouissi N; Zaghloul K; Amraoui A J Fr Ophtalmol; 2001 Nov; 24(9):944-8. PubMed ID: 11912838 [TBL] [Abstract][Full Text] [Related]
17. Treatment of the Weill-Marchesani syndrome. Ritch R; Wand M Ann Ophthalmol; 1981 Jun; 13(6):665-7. PubMed ID: 6455083 [No Abstract] [Full Text] [Related]
19. Weill-Marchesani syndrome with advanced glaucoma and corneal endothelial dysfunction: a case report and literature review. Guo H; Wu X; Cai K; Qiao Z BMC Ophthalmol; 2015 Jan; 15():3. PubMed ID: 25571963 [TBL] [Abstract][Full Text] [Related]
20. Weill-Marchesani syndrome--possible linkage of the autosomal dominant form to 15q21.1. Wirtz MK; Samples JR; Kramer PL; Rust K; Yount J; Acott TS; Koler RD; Cisler J; Jahed A; Gorlin RJ; Godfrey M Am J Med Genet; 1996 Oct; 65(1):68-75. PubMed ID: 8914744 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]