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4. A novel susceptibility locus for moyamoya disease on chromosome 8q23. Sakurai K; Horiuchi Y; Ikeda H; Ikezaki K; Yoshimoto T; Fukui M; Arinami T J Hum Genet; 2004; 49(5):278-81. PubMed ID: 15362573 [TBL] [Abstract][Full Text] [Related]
5. [Preliminary linkage analysis of a Chinese family with benign familial infantile convulsion]. Xiong G; Deng FY; Xiao B; Yang XS; Ning JC; Wu ZG; Wang K; Deng HW Zhonghua Er Ke Za Zhi; 2004 Jun; 42(6):424-8. PubMed ID: 15265426 [TBL] [Abstract][Full Text] [Related]
6. Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Ikeda H; Sasaki T; Yoshimoto T; Fukui M; Arinami T Am J Hum Genet; 1999 Feb; 64(2):533-7. PubMed ID: 9973290 [TBL] [Abstract][Full Text] [Related]
8. Linkage of Gordon's syndrome to the long arm of chromosome 17 in a region recently linked to familial essential hypertension. O'Shaughnessy KM; Fu B; Johnson A; Gordon RD J Hum Hypertens; 1998 Oct; 12(10):675-8. PubMed ID: 9819014 [TBL] [Abstract][Full Text] [Related]
9. A susceptibility locus for epidermodysplasia verruciformis, an abnormal predisposition to infection with the oncogenic human papillomavirus type 5, maps to chromosome 17qter in a region containing a psoriasis locus. Ramoz N; Rueda LA; Bouadjar B; Favre M; Orth G J Invest Dermatol; 1999 Mar; 112(3):259-63. PubMed ID: 10084299 [TBL] [Abstract][Full Text] [Related]
10. Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12. Gadelha MR; Une KN; Rohde K; Vaisman M; Kineman RD; Frohman LA J Clin Endocrinol Metab; 2000 Feb; 85(2):707-14. PubMed ID: 10690880 [TBL] [Abstract][Full Text] [Related]
11. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree. Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197 [TBL] [Abstract][Full Text] [Related]
12. Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions. Weeks DE; Conley YP; Tsai HJ; Mah TS; Rosenfeld PJ; Paul TO; Eller AW; Morse LS; Dailey JP; Ferrell RE; Gorin MB Am J Ophthalmol; 2001 Nov; 132(5):682-92. PubMed ID: 11704029 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Evidence for linkage of the gene causing familial Mediterranean fever to chromosome 17q in non-Ashkenazi Jewish families: second locus or type I error? Aksentijevich I; Gruberg L; Pras E; Balow JE; Kovo M; Gazit E; Dean M; Pras M; Kastner DL Hum Genet; 1993 Jul; 91(6):527-34. PubMed ID: 8340105 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel. Ocaka L; Zhao C; Reed JA; Ebenezer ND; Brice G; Morley T; Mehta M; O'Dowd J; Weber JL; Hardcastle AJ; Child AH J Med Genet; 2008 Feb; 45(2):87-92. PubMed ID: 17932119 [TBL] [Abstract][Full Text] [Related]
17. Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25. Pellegrino JE; George RA; Biegel J; Farlow MR; Gardner K; Caress J; Brown MJ; Rebbeck TR; Bird TD; Chance PF Hum Genet; 1997 Dec; 101(3):277-83. PubMed ID: 9439655 [TBL] [Abstract][Full Text] [Related]
18. A novel locus for Leber congenital amaurosis (LCA4) with anterior keratoconus mapping to chromosome 17p13. Hameed A; Khaliq S; Ismail M; Anwar K; Ebenezer ND; Jordan T; Mehdi SQ; Payne AM; Bhattacharya SS Invest Ophthalmol Vis Sci; 2000 Mar; 41(3):629-33. PubMed ID: 10711674 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes Graves' disease-1 (GD-1) close to multinodular goiter-1 (MNG-1). International Consortium for the Genetics of Autoimmune Thyroid Disease. Tomer Y; Barbesino G; Greenberg DA; Concepcion E; Davies TF J Clin Endocrinol Metab; 1998 Dec; 83(12):4321-7. PubMed ID: 9851771 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]