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)
41. A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse. Aubin I; Adams CP; Opsahl S; Septier D; Bishop CE; Auge N; Salvayre R; Negre-Salvayre A; Goldberg M; Guénet JL; Poirier C Nat Genet; 2005 Aug; 37(8):803-5. PubMed ID: 16025116 [TBL] [Abstract][Full Text] [Related]
42. Validation of a male-specific, 12-locus fluorescent short tandem repeat (STR) multiplex. Krenke BE; Viculis L; Richard ML; Prinz M; Milne SC; Ladd C; Gross AM; Gornall T; Frappier JR; Eisenberg AJ; Barna C; Aranda XG; Adamowicz MS; Budowle B Forensic Sci Int; 2005 Feb; 148(1):1-14. PubMed ID: 15607584 [TBL] [Abstract][Full Text] [Related]
43. [Familial febrile convulsions is supposed to link to human chromosome 19p13.3]. Qi Y; Lü J; Wu X Zhonghua Yi Xue Za Zhi; 2001 Jan; 81(1):27-9. PubMed ID: 11798847 [TBL] [Abstract][Full Text] [Related]
44. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene. Danciger M; Hendrickson J; Lyon J; Toomes C; McHale JC; Fishman GA; Inglehearn CF; Jacobson SG; Farber DB Invest Ophthalmol Vis Sci; 2001 Oct; 42(11):2458-65. PubMed ID: 11581183 [TBL] [Abstract][Full Text] [Related]
45. Quantitative analysis of chimerism after allogeneic stem cell transplantation by real-time polymerase chain reaction with single nucleotide polymorphisms, standard tandem repeats, and Y-chromosome-specific sequences. Koldehoff M; Steckel NK; Hlinka M; Beelen DW; Elmaagacli AH Am J Hematol; 2006 Oct; 81(10):735-46. PubMed ID: 16838323 [TBL] [Abstract][Full Text] [Related]
46. X-linked idiopathic infantile nystagmus associated with a missense mutation in FRMD7. Shiels A; Bennett TM; Prince JB; Tychsen L Mol Vis; 2007 Nov; 13():2233-41. PubMed ID: 18087240 [TBL] [Abstract][Full Text] [Related]
47. Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III. MacDougall M; Zeichner-David M; Murray J; Crall M; Davis A; Slavkin H Am J Hum Genet; 1992 Jan; 50(1):190-4. PubMed ID: 1729887 [TBL] [Abstract][Full Text] [Related]
48. Treatment of dentinogenesis imperfecta in a child: report of case. Nayar AK; Latta JB; Soni NN ASDC J Dent Child; 1981; 48(6):453-5. PubMed ID: 6946089 [No Abstract] [Full Text] [Related]
49. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family. Zhang Q; Guo X; Xiao X; Yi J; Jia X; Hejtmancik JF Mol Vis; 2004 Nov; 10():890-900. PubMed ID: 15570218 [TBL] [Abstract][Full Text] [Related]
50. [Linkage analysis of cytokine and cytokine-related receptor gene loci and essential hypertension in Chinese]. Chu S; Zhu D; Wang G; Xiong M; Jin L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun; 19(3):221-4. PubMed ID: 12048683 [TBL] [Abstract][Full Text] [Related]
51. Dentinogenesis imperfecta type II: case report. Modesto A; Alves AC; Vieira AR; Portella W Braz Dent J; 1996; 7(1):47-52. PubMed ID: 9206354 [TBL] [Abstract][Full Text] [Related]
52. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. Pankratz N; Nichols WC; Uniacke SK; Halter C; Murrell J; Rudolph A; Shults CW; Conneally PM; Foroud T; Hum Mol Genet; 2003 Oct; 12(20):2599-608. PubMed ID: 12925570 [TBL] [Abstract][Full Text] [Related]
53. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23. Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797 [TBL] [Abstract][Full Text] [Related]
54. Dentinogenesis imperfecta type II- genotype and phenotype analyses in three Danish families. Taleb K; Lauridsen E; Daugaard-Jensen J; Nieminen P; Kreiborg S Mol Genet Genomic Med; 2018 May; 6(3):339-349. PubMed ID: 29512331 [TBL] [Abstract][Full Text] [Related]
55. Refined localization of a punctate palmoplantar keratoderma gene to a 5.06-cM region at 15q22.2-15q22.31. Gao M; Yang S; Li M; Yan KL; Jiang YX; Cui Y; Xiao FL; Shen YJ; Chen JJ; Liu JB; Xu SJ; Huang W; Zhang XJ Br J Dermatol; 2005 May; 152(5):874-8. PubMed ID: 15888140 [TBL] [Abstract][Full Text] [Related]
56. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation. Zhang Q; Zulfiqar F; Riazuddin SA; Xiao X; Ahmad Z; Riazuddin S; Hejtmancik JF Mol Vis; 2004 Nov; 10():884-9. PubMed ID: 15570217 [TBL] [Abstract][Full Text] [Related]
57. [The human major histocompatibility complex region is not a major susceptibility locus for Graves disease among the Hans in north of China]. Jin Y; Hu F; Teng W; Ben S; Zhang J; Xiong X; Huang W Zhonghua Yi Xue Za Zhi; 2002 Sep; 82(18):1242-4. PubMed ID: 12425802 [TBL] [Abstract][Full Text] [Related]
58. Dentinogenesis imperfecta. Goodman DB Int J Orthod; 1973 Mar; 11(1):11-6. PubMed ID: 4512282 [No Abstract] [Full Text] [Related]
59. Dentin matrix protein-1, a candidate gene for dentinogenesis imperfecta. MacDougall M; Gu TT; Simmons D Connect Tissue Res; 1996; 35(1-4):267-72. PubMed ID: 9084665 [TBL] [Abstract][Full Text] [Related]