477 related articles for article (PubMed ID: 12642767)
1. Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus.
Justice CM; Miller NH; Marosy B; Zhang J; Wilson AF
Spine (Phila Pa 1976); 2003 Mar; 28(6):589-94. PubMed ID: 12642767
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
Pankratz N; Nichols WC; Uniacke SK; Halter C; Murrell J; Rudolph A; Shults CW; Conneally PM; Foroud T;
Hum Mol Genet; 2003 Oct; 12(20):2599-608. PubMed ID: 12925570
[TBL] [Abstract][Full Text] [Related]
5. Allelic variants of human melatonin 1A receptor in patients with familial adolescent idiopathic scoliosis.
Morcuende JA; Minhas R; Dolan L; Stevens J; Beck J; Wang K; Weinstein SL; Sheffield V
Spine (Phila Pa 1976); 2003 Sep; 28(17):2025-8; discussion 2029. PubMed ID: 12973153
[TBL] [Abstract][Full Text] [Related]
6. Lack of association between the aggrecan gene and familial idiopathic scoliosis.
Marosy B; Justice CM; Nzegwu N; Kumar G; Wilson AF; Miller NH
Spine (Phila Pa 1976); 2006 Jun; 31(13):1420-5. PubMed ID: 16741449
[TBL] [Abstract][Full Text] [Related]
7. A novel locus for familial migraine on Xp22.
Wieser T; Pascual J; Oterino A; Soso M; Barmada M; Gardner KL
Headache; 2010 Jun; 50(6):955-62. PubMed ID: 20412323
[TBL] [Abstract][Full Text] [Related]
8. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
9. Familial high myopia: evidence of an autosomal dominant mode of inheritance and genetic heterogeneity.
Naiglin L; Clayton J; Gazagne C; Dallongeville F; Malecaze F; Calvas P
Ann Genet; 1999; 42(3):140-6. PubMed ID: 10526656
[TBL] [Abstract][Full Text] [Related]
10. Search for linkage to schizophrenia on the X and Y chromosomes.
DeLisi LE; Devoto M; Lofthouse R; Poulter M; Smith A; Shields G; Bass N; Chen G; Vita A; Morganti C
Am J Med Genet; 1994 Jun; 54(2):113-21. PubMed ID: 8074161
[TBL] [Abstract][Full Text] [Related]
11. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
Sander T; Windemuth C; Schulz H; Saar K; Gennaro E; Bianchi A; Zara F; Bulteau C; Kaminska A; Ville D; Cieuta C; Prud'homme JF; Dulac O; Bate L; Gardiner RM; de Haan GJ; Janssen GA; Witte J; Halley DJ; Lindhout D; Wienker TF; Janz D;
Am J Med Genet; 2002 Aug; 114(6):673-8. PubMed ID: 12210286
[TBL] [Abstract][Full Text] [Related]
12. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.
de Kovel CG; Hol FA; Heister JG; Willemen JJ; Sandkuijl LA; Franke B; Padberg GW
J Med Genet; 2004 Sep; 41(9):652-7. PubMed ID: 15342694
[TBL] [Abstract][Full Text] [Related]
13. [The human major histocompatibility complex region is not a major susceptibility locus for Graves disease among the Hans in north of China].
Jin Y; Hu F; Teng W; Ben S; Zhang J; Xiong X; Huang W
Zhonghua Yi Xue Za Zhi; 2002 Sep; 82(18):1242-4. PubMed ID: 12425802
[TBL] [Abstract][Full Text] [Related]
14. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
[TBL] [Abstract][Full Text] [Related]
15. Integration of linkage analyses and disease association studies.
Nemesure BB; He Q; Mendell N
Genet Epidemiol; 1995; 12(6):653-8. PubMed ID: 8787989
[TBL] [Abstract][Full Text] [Related]
16. Identification of candidate regions for familial idiopathic scoliosis.
Miller NH; Justice CM; Marosy B; Doheny KF; Pugh E; Zhang J; Dietz HC; Wilson AF
Spine (Phila Pa 1976); 2005 May; 30(10):1181-7. PubMed ID: 15897833
[TBL] [Abstract][Full Text] [Related]
17. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families.
Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC
Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539
[TBL] [Abstract][Full Text] [Related]
18. Genetic association of complex traits: using idiopathic scoliosis as an example.
Cheng JC; Tang NL; Yeung HY; Miller N
Clin Orthop Relat Res; 2007 Sep; 462():38-44. PubMed ID: 17534191
[TBL] [Abstract][Full Text] [Related]
19. Truncating mutation in the NHS gene: phenotypic heterogeneity of Nance-Horan syndrome in an asian Indian family.
Ramprasad VL; Thool A; Murugan S; Nancarrow D; Vyas P; Rao SK; Vidhya A; Ravishankar K; Kumaramanickavel G
Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):17-23. PubMed ID: 15623749
[TBL] [Abstract][Full Text] [Related]
20. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
Le Ber I; Camuzat A; Berger E; Hannequin D; Laquerrière A; Golfier V; Seilhean D; Viennet G; Couratier P; Verpillat P; Heath S; Camu W; Martinaud O; Lacomblez L; Vercelletto M; Salachas F; Sellal F; Didic M; Thomas-Anterion C; Puel M; Michel BF; Besse C; Duyckaerts C; Meininger V; Campion D; Dubois B; Brice A;
Neurology; 2009 May; 72(19):1669-76. PubMed ID: 19433740
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]