These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 11110973)
21. [Gene mapping on Blepharophimosis Epicanthus Inversus and Ptosis syndrome type I in Chinese family]. Zhang W; Pang H; Shi H; Huang S Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Feb; 18(1):8-10. PubMed ID: 11172632 [TBL] [Abstract][Full Text] [Related]
22. A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family. Xia XY; Cui YX; Huang YF; Pan LJ; Yang B; Wang HY; Li XJ; Shi YC; Lu HY; Zhou YC Clin Chim Acta; 2008 Dec; 398(1-2):148-51. PubMed ID: 18755172 [TBL] [Abstract][Full Text] [Related]
23. [Occurrence of dentinogenesis imperfecta hereditaria (Capdepont's disease) in four successive generations of one family]. Szczepanński M; Uścinowicz M; Kaczmarski M Pediatr Pol; 1995 Aug; 70(8):679-81. PubMed ID: 8668371 [TBL] [Abstract][Full Text] [Related]
24. A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family. Zhang X; Chen L; Liu J; Zhao Z; Qu E; Wang X; Chang W; Xu C; Wang QK; Liu M BMC Med Genet; 2007 Aug; 8():52. PubMed ID: 17686168 [TBL] [Abstract][Full Text] [Related]
25. A genome-wide scan maps a novel juvenile-onset primary open angle glaucoma locus to chromosome 5q. Pang CP; Fan BJ; Canlas O; Wang DY; Dubois S; Tam PO; Lam DS; Raymond V; Ritch R Mol Vis; 2006 Feb; 12():85-92. PubMed ID: 16518310 [TBL] [Abstract][Full Text] [Related]
26. A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32. Sundin OH; Broman KW; Chang HH; Vito EC; Stark WJ; Gottsch JD Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3919-26. PubMed ID: 16936105 [TBL] [Abstract][Full Text] [Related]
27. Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis. Ye X; Shi L; Yin W; Meng L; Wang QK; Bian Z J Clin Periodontol; 2009 Aug; 36(8):627-33. PubMed ID: 19552635 [TBL] [Abstract][Full Text] [Related]
28. Identification of candidate regions for a novel Usher syndrome type II locus. Ben Rebeh I; Benzina Z; Dhouib H; Hadjamor I; Amyere M; Ayadi L; Turki K; Hammami B; Kmiha N; Kammoun H; Hakim B; Charfedine I; Vikkula M; Ghorbel A; Ayadi H; Masmoudi S Mol Vis; 2008 Sep; 14():1719-26. PubMed ID: 18806881 [TBL] [Abstract][Full Text] [Related]
29. [A study on localization of an autosomal dominant retinitis pigmentosa gene]. Ma X; Wei R; Cai J; Zhu L Zhonghua Yan Ke Za Zhi; 2002 Nov; 38(11):680-3. PubMed ID: 12487900 [TBL] [Abstract][Full Text] [Related]
30. [Dentinogenesis imperfecta type II]. Salvolini E; Di Giorgio R; Caselli E; De Florio L Radiol Med; 1998 Nov; 96(5):518-20. PubMed ID: 10051880 [No Abstract] [Full Text] [Related]
31. 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]
32. [Multidisciplinary focus on dentinogenesis imperfecta type II. Clinical analysis. Ultrastructural and genetic pathology]. Rivera H; Terán B; Pinto Cisternas J Acta Odontol Venez; 1990; 28(2-3):49-54. PubMed ID: 2131729 [TBL] [Abstract][Full Text] [Related]
33. Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families. Sukor N; Mulatero P; Gordon RD; So A; Duffy D; Bertello C; Kelemen L; Jeske Y; Veglio F; Stowasser M J Hypertens; 2008 Aug; 26(8):1577-82. PubMed ID: 18622235 [TBL] [Abstract][Full Text] [Related]
34. Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage. Wolf MT; Zalewski I; Martin FC; Ruf R; Müller D; Hennies HC; Schwarz S; Panther F; Attanasio M; Acosta HG; Imm A; Lucke B; Utsch B; Otto E; Nurnberg P; Nieto VG; Hildebrandt F Nephrol Dial Transplant; 2005 May; 20(5):909-14. PubMed ID: 15741201 [TBL] [Abstract][Full Text] [Related]
35. A genome-wide scan maps a novel high myopia locus to 5p15. Lam CY; Tam PO; Fan DS; Fan BJ; Wang DY; Lee CW; Pang CP; Lam DS Invest Ophthalmol Vis Sci; 2008 Sep; 49(9):3768-78. PubMed ID: 18421076 [TBL] [Abstract][Full Text] [Related]
36. A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1. Wang L; Lin H; Shen Y; Huang S; Gu J; Su H; Qi Y Mol Vis; 2007 Aug; 13():1357-62. PubMed ID: 17768382 [TBL] [Abstract][Full Text] [Related]
37. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area. Shih WL; Yu MW; Chen PJ; Yeh SH; Lo MT; Chang HC; Liaw YF; Lin SM; Liu CJ; Lee SD; Lin CL; Hsiao CK; Yang SY; Chen CJ Oncogene; 2006 May; 25(22):3219-24. PubMed ID: 16407824 [TBL] [Abstract][Full Text] [Related]
38. Genetic linkage of snowflake vitreoretinal degeneration to chromosome 2q36. Jiao X; Ritter R; Hejtmancik JF; Edwards AO Invest Ophthalmol Vis Sci; 2004 Dec; 45(12):4498-503. PubMed ID: 15557460 [TBL] [Abstract][Full Text] [Related]
39. Familial Wolff-Parkinson-White syndrome is linked to the loci on chromosome 7q3. Liu W; Liu G; Hu D; Qi Y; Shan Z; Yang D; Liu D; Wang Y Chin Med J (Engl); 2002 Nov; 115(11):1733-5. PubMed ID: 12609097 [TBL] [Abstract][Full Text] [Related]
40. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26. McAuley EZ; Blair IP; Liu Z; Fullerton JM; Scimone A; Van Herten M; Evans MR; Kirkby KC; Donald JA; Mitchell PB; Schofield PR Mol Psychiatry; 2009 May; 14(5):492-500. PubMed ID: 18227837 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]