178 related articles for article (PubMed ID: 12908008)
1. Genome-wide search for strabismus susceptibility loci.
Fujiwara H; Matsuo T; Sato M; Yamane T; Kitada M; Hasebe S; Ohtsuki H
Acta Med Okayama; 2003 Jun; 57(3):109-16. PubMed ID: 12908008
[TBL] [Abstract][Full Text] [Related]
2. Chromosomes 4q28.3 and 7q31.2 as new susceptibility loci for comitant strabismus.
Shaaban S; Matsuo T; Fujiwara H; Itoshima E; Furuse T; Hasebe S; Zhang Q; Ott J; Ohtsuki H
Invest Ophthalmol Vis Sci; 2009 Feb; 50(2):654-61. PubMed ID: 18824738
[TBL] [Abstract][Full Text] [Related]
3. Two-stage genome-wide linkage scan in keratoconus sib pair families.
Li X; Rabinowitz YS; Tang YG; Picornell Y; Taylor KD; Hu M; Yang H
Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3791-5. PubMed ID: 16936089
[TBL] [Abstract][Full Text] [Related]
4. Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.
Panhuysen CI; Karban A; Knodle Manning A; Bayless TM; Duerr RH; Bailey-Wilson JE; Epstein EH; Brant SR
Hum Genet; 2006 Aug; 120(1):31-41. PubMed ID: 16733713
[TBL] [Abstract][Full Text] [Related]
5. Linkage of hypertension to chromosome 2q14-q23 in Chinese families.
Zhu DL; Wang HY; Xiong MM; He X; Chu SL; Jin L; Wang GL; Yuan WT; Zhao GS; Boerwinkle E; Huang W
J Hypertens; 2001 Jan; 19(1):55-61. PubMed ID: 11204305
[TBL] [Abstract][Full Text] [Related]
6. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen-White KR; Rosso A; Donald JA; Adams LJ; Schofield PR
Mol Psychiatry; 2002; 7(8):851-9. PubMed ID: 12232778
[TBL] [Abstract][Full Text] [Related]
7. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen-White KR; Rosso A; Donald JA; Adams LJ; Schofield PR
Mol Psychiatry; 2002; 7(6):594-603. PubMed ID: 12140782
[TBL] [Abstract][Full Text] [Related]
8. Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome.
Khan AO; Shinwari J; Al Sharif L; Khalil D; Al-Gehedan S; Tassan NA
Mol Vis; 2011; 17():1997-2002. PubMed ID: 21850174
[TBL] [Abstract][Full Text] [Related]
9. [Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia].
Zeng LP; Hu ZM; Mu LL; Mei GS; Lu XL; Zheng YJ; Li PJ; Zhang YX; Pan Q; Long ZG; Dai HP; Zhang ZH; Xia JH; Zhao JP; Xia K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):256-60. PubMed ID: 21644218
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12.
Stambolian D; Ibay G; Reider L; Dana D; Moy C; Schlifka M; Holmes TN; Ciner E; Bailey-Wilson JE
Mol Vis; 2006 Dec; 12():1499-505. PubMed ID: 17167407
[TBL] [Abstract][Full Text] [Related]
11. Investigation of parent-of-origin effect in comitant strabismus using MOD score analysis.
Shaaban S; Matsuo T; Strauch K; Ohtsuki H
Mol Vis; 2009 Jun; 15():1351-8. PubMed ID: 19597570
[TBL] [Abstract][Full Text] [Related]
12. Genome-wide linkage screen for testicular germ cell tumour susceptibility loci.
Crockford GP; Linger R; Hockley S; Dudakia D; Johnson L; Huddart R; Tucker K; Friedlander M; Phillips KA; Hogg D; Jewett MA; Lohynska R; Daugaard G; Richard S; Chompret A; Bonaïti-Pellié C; Heidenreich A; Albers P; Olah E; Geczi L; Bodrogi I; Ormiston WJ; Daly PA; Guilford P; Fosså SD; Heimdal K; Tjulandin SA; Liubchenko L; Stoll H; Weber W; Forman D; Oliver T; Einhorn L; McMaster M; Kramer J; Greene MH; Weber BL; Nathanson KL; Cortessis V; Easton DF; Bishop DT; Stratton MR; Rapley EA
Hum Mol Genet; 2006 Feb; 15(3):443-51. PubMed ID: 16407372
[TBL] [Abstract][Full Text] [Related]
13. Linkage analysis of high myopia susceptibility locus in 26 families.
Paget S; Julia S; Vitezica ZG; Soler V; Malecaze F; Calvas P
Mol Vis; 2008; 14():2566-74. PubMed ID: 19122830
[TBL] [Abstract][Full Text] [Related]
14. Replication of the recessive STBMS1 locus but with dominant inheritance.
Rice A; Nsengimana J; Simmons IG; Toomes C; Hoole J; Willoughby CE; Cassidy F; Williams GA; George ND; Sheridan E; Young TL; Hunter TI; Barrett BT; Elliott DB; Bishop DT; Inglehearn CF
Invest Ophthalmol Vis Sci; 2009 Jul; 50(7):3210-7. PubMed ID: 19218600
[TBL] [Abstract][Full Text] [Related]
15. Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.
Vionnet N; Hani EH; Dupont S; Gallina S; Francke S; Dotte S; De Matos F; Durand E; Leprêtre F; Lecoeur C; Gallina P; Zekiri L; Dina C; Froguel P
Am J Hum Genet; 2000 Dec; 67(6):1470-80. PubMed ID: 11067779
[TBL] [Abstract][Full Text] [Related]
16. A genome-wide autosomal screen for schizophrenia susceptibility loci in 71 families with affected siblings: support for loci on chromosome 10p and 6.
Schwab SG; Hallmayer J; Albus M; Lerer B; Eckstein GN; Borrmann M; Segman RH; Hanses C; Freymann J; Yakir A; Trixler M; Falkai P; Rietschel M; Maier W; Wildenauer DB
Mol Psychiatry; 2000 Nov; 5(6):638-49. PubMed ID: 11126394
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3.
Van Vlijmen-Van Keulen CJ; Rauwerda JA; Pals G
Eur J Vasc Endovasc Surg; 2005 Jul; 30(1):29-35. PubMed ID: 15933979
[TBL] [Abstract][Full Text] [Related]
18. A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer.
Djureinovic T; Skoglund J; Vandrovcova J; Zhou XL; Kalushkova A; Iselius L; Lindblom A
Gut; 2006 Mar; 55(3):362-6. PubMed ID: 16150854
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Genome gender diversity in affected sib-pairs with familial vesico-ureteric reflux identified by single nucleotide polymorphism linkage analysis.
Marchini GS; Onal B; Guo CY; Rowe CK; Kunkel L; Bauer SB; Retik AB; Nguyen HT
BJU Int; 2012 Jun; 109(11):1709-14. PubMed ID: 21981614
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
