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4. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN). Oetting WS; Armstrong CM; Holleschau AM; DeWan AT; Summers GC Ophthalmic Genet; 2000 Dec; 21(4):227-33. PubMed ID: 11135493 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Mapping of an autosomal dominant gene for Dupuytren's contracture to chromosome 16q in a Swedish family. Hu FZ; Nystrom A; Ahmed A; Palmquist M; Dopico R; Mossberg I; Gladitz J; Rayner M; Post JC; Ehrlich GD; Preston RA Clin Genet; 2005 Nov; 68(5):424-9. PubMed ID: 16207209 [TBL] [Abstract][Full Text] [Related]
8. A new locus for coeliac disease mapped to chromosome 15 in a population isolate. Woolley N; Holopainen P; Ollikainen V; Mustalahti K; Mäki M; Kere J; Partanen J Hum Genet; 2002 Jul; 111(1):40-5. PubMed ID: 12136234 [TBL] [Abstract][Full Text] [Related]
9. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Lee H; Jen JC; Wang H; Chen Z; Mamsa H; Sabatti C; Baloh RW; Nelson SF Hum Mol Genet; 2006 Jan; 15(2):251-8. PubMed ID: 16330481 [TBL] [Abstract][Full Text] [Related]
10. Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1. Levchenko A; Montplaisir JY; Asselin G; Provost S; Girard SL; Xiong L; Lemyre E; St-Onge J; Thibodeau P; Desautels A; Turecki G; Gaspar C; Dubé MP; Rouleau GA Mov Disord; 2009 Jan; 24(1):40-50. PubMed ID: 18946881 [TBL] [Abstract][Full Text] [Related]
11. Fifth finger camptodactyly maps to chromosome 3q11.2-q13.12 in a large German kindred. Malik S; Schott J; Schiller J; Junge A; Baum E; Koch MC Eur J Hum Genet; 2008 Feb; 16(2):265-9. PubMed ID: 18000522 [TBL] [Abstract][Full Text] [Related]
14. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24. Schüle R; Bonin M; Dürr A; Forlani S; Sperfeld AD; Klimpe S; Mueller JC; Seibel A; van de Warrenburg BP; Bauer P; Schöls L Neurology; 2009 Jun; 72(22):1893-8. PubMed ID: 19357379 [TBL] [Abstract][Full Text] [Related]
15. Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5. Everett KV; Chung EM J Hum Genet; 2013 Apr; 58(4):236-7. PubMed ID: 23426030 [TBL] [Abstract][Full Text] [Related]
16. 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]
18. 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]
19. No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric Stenosis. Lagerstedt-Robinson K; Svenningsson A; Nordenskjöld A J Hum Genet; 2009 Dec; 54(12):706-8. PubMed ID: 19851341 [TBL] [Abstract][Full Text] [Related]
20. Suggestive linkage of schizophrenia to 5p13 in Costa Rica. Cooper-Casey K; Mésen-Fainardi A; Galke-Rollins B; Llach M; Laprade B; Rodriguez C; Riondet S; Bertheau A; Byerley W Mol Psychiatry; 2005 Jul; 10(7):651-6. PubMed ID: 15700049 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]