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22. A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34. Moynihan L; Jackson AP; Roberts E; Karbani G; Lewis I; Corry P; Turner G; Mueller RF; Lench NJ; Woods CG Am J Hum Genet; 2000 Feb; 66(2):724-7. PubMed ID: 10677332 [TBL] [Abstract][Full Text] [Related]
23. Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalities. Bidinost C; Matsumoto M; Chung D; Salem N; Zhang K; Stockton DW; Khoury A; Megarbane A; Bejjani BA; Traboulsi EI Invest Ophthalmol Vis Sci; 2006 Apr; 47(4):1274-80. PubMed ID: 16565358 [TBL] [Abstract][Full Text] [Related]
24. A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23. Dick KJ; Al-Mjeni R; Baskir W; Koul R; Simpson MA; Patton MA; Raeburn S; Crosby AH Neurology; 2008 Jul; 71(4):248-52. PubMed ID: 18463364 [TBL] [Abstract][Full Text] [Related]
25. A new locus for a childhood onset, slowly progressive autosomal recessive spinocerebellar ataxia maps to chromosome 11p15. Breedveld GJ; van Wetten B; te Raa GD; Brusse E; van Swieten JC; Oostra BA; Maat-Kievit JA J Med Genet; 2004 Nov; 41(11):858-66. PubMed ID: 15520412 [No Abstract] [Full Text] [Related]
26. A locus for autosomal recessive pseudoxanthoma elasticum, with penetrance of vascular symptoms in carriers, maps to chromosome 16p13.1. van Soest S; Swart J; Tijmes N; Sandkuijl LA; Rommers J; Bergen AA Genome Res; 1997 Aug; 7(8):830-4. PubMed ID: 9267806 [TBL] [Abstract][Full Text] [Related]
27. Linkage mapping of ovine microphthalmia to chromosome 23, the sheep orthologue of human chromosome 18. Tetens J; Ganter M; Müller G; Drögemüller C Invest Ophthalmol Vis Sci; 2007 Aug; 48(8):3506-15. PubMed ID: 17652717 [TBL] [Abstract][Full Text] [Related]
32. Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3-34.13. Klar J; Gedde-Dahl T; Larsson M; Pigg M; Carlsson B; Tentler D; Vahlquist A; Dahl N J Med Genet; 2004 Mar; 41(3):208-12. PubMed ID: 14985385 [No Abstract] [Full Text] [Related]
33. 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]
34. A genome-wide scan maps a novel juvenile-onset primary open-angle glaucoma locus to 15q. Wang DY; Fan BJ; Chua JK; Tam PO; Leung CK; Lam DS; Pang CP Invest Ophthalmol Vis Sci; 2006 Dec; 47(12):5315-21. PubMed ID: 17122119 [TBL] [Abstract][Full Text] [Related]
37. Bipolar affective disorder, chromosome 16p13.3, and recessive disease genes. Ewald H; Kruse TA Am J Med Genet; 1997 Sep; 74(5):549-50. PubMed ID: 9342211 [No Abstract] [Full Text] [Related]
38. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3. Tariq M; Chishti MS; Ali G; Ahmad W Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143 [TBL] [Abstract][Full Text] [Related]
39. Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25. Visapää I; Salonen R; Varilo T; Paavola P; Peltonen L Am J Hum Genet; 1999 Oct; 65(4):1086-95. PubMed ID: 10486328 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]