149 related articles for article (PubMed ID: 16098013)
21. Analysis of mutations in the SOS-1 gene in two Polish families with hereditary gingival fibromatosis.
Gawron K; Bereta G; Nowakowska Z; Łazarz-Bartyzel K; Potempa J; Chomyszyn-Gajewska M; Górska R; Plakwicz P
Oral Dis; 2017 Oct; 23(7):983-989. PubMed ID: 28425619
[TBL] [Abstract][Full Text] [Related]
22. ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm.
Rampazzo A; Nava A; Miorin M; Fonderico P; Pope B; Tiso N; Livolsi B; Zimbello R; Thiene G; Danieli GA
Genomics; 1997 Oct; 45(2):259-63. PubMed ID: 9344647
[TBL] [Abstract][Full Text] [Related]
23. Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis.
Chen J; Xu X; Chen S; Lu T; Zheng Y; Gan Z; Shen Z; Ma S; Wang D; Su L; He F; Shang X; Xu H; Chen D; Zhang L; Xiong F
Int J Oral Sci; 2023 Sep; 15(1):46. PubMed ID: 37752101
[TBL] [Abstract][Full Text] [Related]
24. Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.
Hazan J; Fontaine B; Bruyn RP; Lamy C; van Deutekom JC; Rime CS; Dürr A; Melki J; Lyon-Caen O; Agid Y
Hum Mol Genet; 1994 Sep; 3(9):1569-73. PubMed ID: 7833913
[TBL] [Abstract][Full Text] [Related]
25. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.
De Michele G; De Fusco M; Cavalcanti F; Filla A; Marconi R; Volpe G; Monticelli A; Ballabio A; Casari G; Cocozza S
Am J Hum Genet; 1998 Jul; 63(1):135-9. PubMed ID: 9634528
[TBL] [Abstract][Full Text] [Related]
26. [A genome-wide screening for pathological myopia suggests a novel locus on chromosome 15q12 - 13].
Yu ZQ; Li YB; Huang CX; Chu RY; Hu DN; Shen ZH; Huang W
Zhonghua Yan Ke Za Zhi; 2007 Mar; 43(3):233-8. PubMed ID: 17605906
[TBL] [Abstract][Full Text] [Related]
27. Characterization of fibroblasts with Son of Sevenless-1 mutation.
Lee EJ; Jang SI; Pallos D; Kather J; Hart TC
J Dent Res; 2006 Nov; 85(11):1050-5. PubMed ID: 17062749
[TBL] [Abstract][Full Text] [Related]
28. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2.
Irshad S; Santos RL; Muhammad D; Lee K; McArthur N; Haque S; Ahmad W; Leal SM
Clin Genet; 2005 Sep; 68(3):262-7. PubMed ID: 16098016
[TBL] [Abstract][Full Text] [Related]
29. A new locus for autosomal dominant congenital coronary cataract in a Chinese family maps to chromosome 3q.
Liu G; Li Y; Ruan Y; Cao W; Xin L; Qian J; Gu J
Mol Vis; 2010 May; 16():874-9. PubMed ID: 20508730
[TBL] [Abstract][Full Text] [Related]
30. Sequence analysis of the Ras-MAPK pathway genes SOS1, EGFR & GRB2 in silver foxes (Vulpes vulpes): candidate genes for hereditary hyperplastic gingivitis.
Clark JA; Tully SJ; Dawn Marshall H
Genetica; 2014 Dec; 142(6):517-23. PubMed ID: 25377643
[TBL] [Abstract][Full Text] [Related]
31. Evidence for a novel autosomal dominant retinitis pigmentosa linked to chromosome 1p22.1-q12 in a Chinese family.
Yuan Y; Zhou X; Wang F; Yan M; Ding F
Curr Eye Res; 2011 Feb; 36(2):154-67. PubMed ID: 21281067
[TBL] [Abstract][Full Text] [Related]
32. Assignment of a locus (GLC3A) for primary congenital glaucoma (Buphthalmos) to 2p21 and evidence for genetic heterogeneity.
Sarfarazi M; Akarsu AN; Hossain A; Turacli ME; Aktan SG; Barsoum-Homsy M; Chevrette L; Sayli BS
Genomics; 1995 Nov; 30(2):171-7. PubMed ID: 8586416
[TBL] [Abstract][Full Text] [Related]
33. Evidence for a nonallelic heterogeneity of epidermodysplasia verruciformis with two susceptibility loci mapped to chromosome regions 2p21-p24 and 17q25.
Ramoz N; Taïeb A; Rueda LA; Montoya LS; Bouadjar B; Favre M; Orth G
J Invest Dermatol; 2000 Jun; 114(6):1148-53. PubMed ID: 10844558
[TBL] [Abstract][Full Text] [Related]
34. Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.
Malik S; Grzeschik KH
Hum Genet; 2008 Mar; 123(2):197-205. PubMed ID: 18193458
[TBL] [Abstract][Full Text] [Related]
35. Hereditary gingival fibromatosis: characteristics and novel putative pathogenic mechanisms.
Häkkinen L; Csiszar A
J Dent Res; 2007 Jan; 86(1):25-34. PubMed ID: 17189459
[TBL] [Abstract][Full Text] [Related]
36. A novel locus of coralliform cataract mapped to chromosome 2p24-pter.
Gao L; Qin W; Cui H; Feng G; Liu P; Gao W; Ma L; Li P; He L; Fu S
J Hum Genet; 2005; 50(6):305-310. PubMed ID: 15933805
[TBL] [Abstract][Full Text] [Related]
37. A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1-q22.3.
Xing Q; Chen X; Wang M; Bai W; Peng X; Gao R; Wu S; Qian X; Qin W; Gao J; Feng G; He L
Hum Genet; 2005 Jul; 117(2-3):154-9. PubMed ID: 15841387
[TBL] [Abstract][Full Text] [Related]
38. Researchers discover gene mutation responsible for hereditary gingival fibromatosis.
Dent Today; 2002 May; 21(5):38-9. PubMed ID: 12026713
[No Abstract] [Full Text] [Related]
39. A locus for migraine without aura maps on chromosome 14q21.2-q22.3.
Soragna D; Vettori A; Carraro G; Marchioni E; Vazza G; Bellini S; Tupler R; Savoldi F; Mostacciuolo ML
Am J Hum Genet; 2003 Jan; 72(1):161-7. PubMed ID: 12474141
[TBL] [Abstract][Full Text] [Related]
40. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Ashley-Koch A; Bonner ER; Gaskell PC; West SG; Tim R; Wolpert CM; Jones R; Farrell CD; Nance M; Svenson IK; Marchuk DA; Boustany RM; Vance JM; Scott WK; Pericak-Vance MA
Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]