125 related articles for article (PubMed ID: 9439671)
1. Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping.
Laass MW; Hennies HC; Preis S; Stevens HP; Jung M; Leigh IM; Wienker TF; Reis A
Hum Genet; 1997 Dec; 101(3):376-82. PubMed ID: 9439671
[TBL] [Abstract][Full Text] [Related]
2. Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region.
Fischer J; Blanchet-Bardon C; Prud'homme JF; Pavek S; Steijlen PM; Dubertret L; Weissenbach J
Eur J Hum Genet; 1997; 5(3):156-60. PubMed ID: 9272739
[TBL] [Abstract][Full Text] [Related]
3. Sublocalization of the Papillon-Lefevre syndrome locus on 11q14-q21.
Hart TC; Bowden DW; Ghaffar KA; Wang W; Cutler CW; Cebeci I; Efeoglu A; Firatli E
Am J Med Genet; 1998 Sep; 79(2):134-9. PubMed ID: 9741471
[TBL] [Abstract][Full Text] [Related]
4. Genetic studies of syndromes with severe periodontitis and palmoplantar hyperkeratosis.
Hart TC; Stabholz A; Meyle J; Shapira L; Van Dyke TE; Cutler CW; Soskolne WA
J Periodontal Res; 1997 Jan; 32(1 Pt 2):81-9. PubMed ID: 9085215
[TBL] [Abstract][Full Text] [Related]
5. Loss-of-function mutations in the cathepsin C gene result in periodontal disease and palmoplantar keratosis.
Toomes C; James J; Wood AJ; Wu CL; McCormick D; Lench N; Hewitt C; Moynihan L; Roberts E; Woods CG; Markham A; Wong M; Widmer R; Ghaffar KA; Pemberton M; Hussein IR; Temtamy SA; Davies R; Read AP; Sloan P; Dixon MJ; Thakker NS
Nat Genet; 1999 Dec; 23(4):421-4. PubMed ID: 10581027
[TBL] [Abstract][Full Text] [Related]
6. Localisation of a gene for prepubertal periodontitis to chromosome 11q14 and identification of a cathepsin C gene mutation.
Hart TC; Hart PS; Michalec MD; Zhang Y; Marazita ML; Cooper M; Yassin OM; Nusier M; Walker S
J Med Genet; 2000 Feb; 37(2):95-101. PubMed ID: 10662808
[TBL] [Abstract][Full Text] [Related]
7. Papillon-Lefèvre syndrome: mutations and polymorphisms in the cathepsin C gene.
Nakano A; Nomura K; Nakano H; Ono Y; LaForgia S; Pulkkinen L; Hashimoto I; Uitto J
J Invest Dermatol; 2001 Feb; 116(2):339-43. PubMed ID: 11180012
[TBL] [Abstract][Full Text] [Related]
8. Novel point mutations, deletions, and polymorphisms in the cathepsin C gene in nine families from Europe and North Africa with Papillon-Lefèvre syndrome.
Lefèvre C; Blanchet-Bardon C; Jobard F; Bouadjar B; Stalder JF; Cure S; Hoffmann A; Prud'Homme JF; Fischer J
J Invest Dermatol; 2001 Dec; 117(6):1657-61. PubMed ID: 11886537
[TBL] [Abstract][Full Text] [Related]
9. Papillon-Lefèvre syndrome: report of six patients and identification of a novel mutation.
Tekin B; Yucelten D; Beleggia F; Sarig O; Sprecher E
Int J Dermatol; 2016 Aug; 55(8):898-902. PubMed ID: 27062382
[TBL] [Abstract][Full Text] [Related]
10. Papillon Lefevre syndrome.
Thomas S; Gummadapu S; Ahsan A; Pai KM
Saudi Med J; 2004 Jul; 25(7):941-3. PubMed ID: 15235704
[TBL] [Abstract][Full Text] [Related]
11. Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome.
Hart TC; Hart PS; Bowden DW; Michalec MD; Callison SA; Walker SJ; Zhang Y; Firatli E
J Med Genet; 1999 Dec; 36(12):881-7. PubMed ID: 10593994
[TBL] [Abstract][Full Text] [Related]
12. Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C.
Hart TC; Hart PS; Michalec MD; Zhang Y; Firatli E; Van Dyke TE; Stabholz A; Zlotogorski A; Shapira L; Soskolne WA
J Med Genet; 2000 Feb; 37(2):88-94. PubMed ID: 10662807
[TBL] [Abstract][Full Text] [Related]
13. Papillon-Lefèvre syndrome: report of three cases in the same family.
Keskin-Yildirim Z; Simşek-Derelioğlu S; Kantarci M; Yilmaz Y; Büyükavci M
Turk J Pediatr; 2012; 54(2):171-6. PubMed ID: 22734305
[TBL] [Abstract][Full Text] [Related]
14. [Recurrent European missense mutation in a Hungarian pedigree with Papillon-Lefèvre syndrome].
Vályi P; Farkas K; Tripolszki K; Sulák A; Széll M; Nagy N; Nagy K
Fogorv Sz; 2014 Sep; 107(3):87-92. PubMed ID: 25509509
[TBL] [Abstract][Full Text] [Related]
15. Partial expression of the Papillon-Lefèvre syndrome in 2 unrelated families.
Soskolne WA; Stabholz A; van Dyke TE; Hart TC; Meyle J
J Clin Periodontol; 1996 Aug; 23(8):764-9. PubMed ID: 8877663
[TBL] [Abstract][Full Text] [Related]
16. Papillon-Lefevre syndrome: a report of two cases.
Hegde R; Reddy R
J Indian Soc Pedod Prev Dent; 2002 Mar; 20(1):9-11. PubMed ID: 12435026
[TBL] [Abstract][Full Text] [Related]
17. Papillon-Lefevre syndrome. A report of six cases in one family.
Pareek SS; Al-Aska AK
Int J Dermatol; 1986 Dec; 25(10):638-41. PubMed ID: 2948927
[TBL] [Abstract][Full Text] [Related]
18. Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity.
Christodoulou K; Tsingis M; Deymeer F; Serdaroglu P; Ozdemir C; Al-Shehab A; Bairactaris C; Mavromatis I; Mylonas I; Evoli A; Kyriallis K; Middleton LT
Hum Mol Genet; 1997 Apr; 6(4):635-40. PubMed ID: 9097970
[TBL] [Abstract][Full Text] [Related]
19. Papillon-Lefèvre syndrome with homozygous nonsense mutation of cathepsin C gene presenting with late-onset periodontitis.
Ragunatha S; Ramesh M; Anupama P; Kapoor M; Bhat M
Pediatr Dermatol; 2015; 32(2):292-4. PubMed ID: 24894642
[TBL] [Abstract][Full Text] [Related]
20. A novel dysmorphic syndrome with open calvarial sutures and sutural cataracts maps to chromosome 14q13-q21.
Boyadjiev SA; Justice CM; Eyaid W; McKusick VA; Lachman RS; Chowdry AB; Jabak M; Zwaan J; Wilson AF; Jabs EW
Hum Genet; 2003 Jul; 113(1):1-9. PubMed ID: 12677423
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
