184 related articles for article (PubMed ID: 11519376)
41. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
Wali A; Chishti M; Ayub M; Yasinzai M; Kafaitullah ; Ali G; John P; Ahmad W
Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
[TBL] [Abstract][Full Text] [Related]
42. An autosomal genome-wide screen for celiac disease in Bedouin families.
Ding YC; Weizman Z; Yerushalmi B; Elbedour K; Garner CP; Neuhausen SL
Genes Immun; 2008 Jan; 9(1):81-6. PubMed ID: 17943142
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24.
Lerer B; Segman RH; Hamdan A; Kanyas K; Karni O; Kohn Y; Korner M; Lanktree M; Kaadan M; Turetsky N; Yakir A; Kerem B; Macciardi F
Mol Psychiatry; 2003 May; 8(5):488-98. PubMed ID: 12808429
[TBL] [Abstract][Full Text] [Related]
45. Dyschromatosis universalis hereditaria: evidence for autosomal recessive inheritance and identification of a new locus on chromosome 12q21-q23.
Stuhrmann M; Hennies HC; Bukhari IA; Brakensiek K; Nürnberg G; Becker C; Huebener J; Miranda MC; Frye-Boukhriss H; Knothe S; Schmidtke J; El-Harith EH
Clin Genet; 2008 Jun; 73(6):566-72. PubMed ID: 18462451
[TBL] [Abstract][Full Text] [Related]
46. Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.
Vanita V; Hejtmancik JF; Hennies HC; Guleria K; Nürnberg P; Singh D; Sperling K; Singh JR
Mol Vis; 2006 Feb; 12():93-9. PubMed ID: 16518306
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
Mustapha M; Chouery E; Chardenoux S; Naboulsi M; Paronnaud J; Lemainque A; Mégarbané A; Loiselet J; Weil D; Lathrop M; Petit C
Eur J Hum Genet; 2002 Mar; 10(3):210-2. PubMed ID: 11973626
[TBL] [Abstract][Full Text] [Related]
49. 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]
50. Mapping of the human CP49 gene and identification of an intragenic polymorphic marker to allow genetic linkage analysis in autosomal dominant congenital cataract.
Carter JM; McLean WH; West S; Quinlan RA
Biochem Biophys Res Commun; 2000 Apr; 270(2):432-6. PubMed ID: 10753642
[TBL] [Abstract][Full Text] [Related]
51. A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.
Pillai SG; Chiano MN; White NJ; Speer M; Barnes KC; Carlsen K; Gerritsen J; Helms P; Lenney W; Silverman M; Sly P; Sundy J; Tsanakas J; von Berg A; Whyte M; Varsani S; Skelding P; Hauser M; Vance J; Pericak-Vance M; Burns DK; Middleton LT; Brewster SR; Anderson WH; Riley JH
Eur J Hum Genet; 2006 Mar; 14(3):307-16. PubMed ID: 16391567
[TBL] [Abstract][Full Text] [Related]
52. 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]
53. 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]
54. A progressive early onset cataract gene maps to human chromosome 17q24.
Armitage MM; Kivlin JD; Ferrell RE
Nat Genet; 1995 Jan; 9(1):37-40. PubMed ID: 7704021
[TBL] [Abstract][Full Text] [Related]
55. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers.
Masmoudi S; Charfedine I; Rebeh IB; Rebai A; Tlili A; Ghorbel AM; Belguith H; Petit C; Drira M; Ayadi H
Clin Genet; 2004 Oct; 66(4):358-64. PubMed ID: 15355440
[TBL] [Abstract][Full Text] [Related]
56. Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mapping.
Gelb BD; Edelson JG; Desnick RJ
Nat Genet; 1995 Jun; 10(2):235-7. PubMed ID: 7663521
[TBL] [Abstract][Full Text] [Related]
57. Shadow autozygosity mapping by linkage exclusion (SAMPLE): a simple strategy to identify the genetic basis of lethal autosomal recessive disorders.
Carr IM; Szymanska K; Sheridan E; Markham AF; Bonthron DT; Johnson CA
Hum Mutat; 2009 Dec; 30(12):1642-9. PubMed ID: 19842213
[TBL] [Abstract][Full Text] [Related]
58. Giant axonal neuropathy locus refinement to a < 590 kb critical interval.
Cavalier L; BenHamida C; Amouri R; Belal S; Bomont P; Lagarde N; Gressin L; Callen D; Demir E; Topaloglu H; Landrieu P; Ioos C; Hamida MB; Koenig M; Hentati F
Eur J Hum Genet; 2000 Jul; 8(7):527-34. PubMed ID: 10909853
[TBL] [Abstract][Full Text] [Related]
59. Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32.
Nichols WC; Koller DL; Slovis B; Foroud T; Terry VH; Arnold ND; Siemieniak DR; Wheeler L; Phillips JA; Newman JH; Conneally PM; Ginsburg D; Loyd JE
Nat Genet; 1997 Mar; 15(3):277-80. PubMed ID: 9054941
[TBL] [Abstract][Full Text] [Related]
60. Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16.
Sidjanin DJ; Grimes PA; Pretsch W; Neuhäuser-Klaus A; Favor J; Stambolian DE
Invest Ophthalmol Vis Sci; 1997 Nov; 38(12):2502-7. PubMed ID: 9375568
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]