BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 11519376)

  • 81. Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.
    Teltsh O; Kanyas K; Karni O; Levi A; Korner M; Ben-Asher E; Lancet D; Hamdan A; Lerer B; Kohn Y
    Am J Med Genet B Neuropsychiatr Genet; 2008 Mar; 147B(2):209-15. PubMed ID: 17823922
    [TBL] [Abstract][Full Text] [Related]  

  • 82. A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder.
    Ewald H; Wikman FP; Teruel BM; Buttenschön HN; Torralba M; Als TD; El Daoud A; Flint TJ; Jorgensen TH; Blanco L; Kruse TA; Orntoft TF; Mors O
    Am J Med Genet B Neuropsychiatr Genet; 2005 Feb; 133B(1):25-30. PubMed ID: 15558715
    [TBL] [Abstract][Full Text] [Related]  

  • 83. A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.
    Hmani-Aifa M; Ben Salem S; Benzina Z; Bouassida W; Messaoud R; Turki K; Khairallah M; Rebaï A; Fakhfekh F; Söderkvist P; Ayadi H
    Hum Genet; 2009 Oct; 126(4):575-87. PubMed ID: 19526372
    [TBL] [Abstract][Full Text] [Related]  

  • 84. A locus for autosomal dominant posterior polar cataract on chromosome 1p.
    Ionides AC; Berry V; Mackay DS; Moore AT; Bhattacharya SS; Shiels A
    Hum Mol Genet; 1997 Jan; 6(1):47-51. PubMed ID: 9002669
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpoint.
    Walder RY; Shalev H; Brennan TM; Carmi R; Elbedour K; Scott DA; Hanauer A; Mark AL; Patil S; Stone EM; Sheffield VC
    Hum Mol Genet; 1997 Sep; 6(9):1491-7. PubMed ID: 9285786
    [TBL] [Abstract][Full Text] [Related]  

  • 86. [Mapping of a pedigree with autosomal dominant inherited congenital sutural cataract].
    Zhang L; Gao LH; Liu P; Li ZJ; Gao WQ; Qin W; Feng GY; Fu SB; He L
    Zhonghua Yan Ke Za Zhi; 2006 Oct; 42(10):908-12. PubMed ID: 17217785
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.
    Hughes AE; Dash DP; Jackson AJ; Frazer DG; Silvestri G
    Invest Ophthalmol Vis Sci; 2003 Dec; 44(12):5063-6. PubMed ID: 14638698
    [TBL] [Abstract][Full Text] [Related]  

  • 88. An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds.
    Scott DA; Carmi R; Elbedour K; Yosefsberg S; Stone EM; Sheffield VC
    Am J Hum Genet; 1996 Aug; 59(2):385-91. PubMed ID: 8755925
    [TBL] [Abstract][Full Text] [Related]  

  • 89. The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27.
    Leegwater PA; Könst AA; Kuyt B; Sandkuijl LA; Naidu S; Oudejans CB; Schutgens RB; Pronk JC; van der Knaap MS
    Am J Hum Genet; 1999 Sep; 65(3):728-34. PubMed ID: 10441579
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene.
    el-Shanti H; Murray JC; Semina EV; Beutow KH; Scherpbier T; al-Alami J
    Eur J Hum Genet; 1998; 6(3):251-6. PubMed ID: 9781029
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions.
    Génin E; Todorov AA; Clerget-Darpoux F
    Ann Hum Genet; 1998 Sep; 62(Pt 5):419-29. PubMed ID: 10088039
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Anterior polar cataract: clinical spectrum and genetic linkage in a single family.
    Ionides A; Berry V; Mackay D; Shiels A; Bhattacharya S; Moore A
    Eye (Lond); 1998; 12 ( Pt 2)():224-6. PubMed ID: 9683943
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Infantile bilateral striatal necrosis maps to chromosome 19q.
    Basel-Vanagaite L; Straussberg R; Ovadia H; Kaplan A; Magal N; Shorer Z; Shalev H; Walsh C; Shohat M
    Neurology; 2004 Jan; 62(1):87-90. PubMed ID: 14718703
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Autosomal linkage analysis of a Japanese single multiplex schizophrenia pedigree reveals two candidate loci on chromosomes 4q and 3q.
    Kaneko N; Muratake T; Kuwabara H; Kurosaki T; Takei M; Ohtsuki T; Arinami T; Tsuji S; Someya T
    Am J Med Genet B Neuropsychiatr Genet; 2007 Sep; 144B(6):735-42. PubMed ID: 17671967
    [TBL] [Abstract][Full Text] [Related]  

  • 95. [Gene mapping in a Chinese family with autosomal dominant centralpuiverulent cataract].
    Li ND; Bu J; Yuan ST; Yang JJ; Zhao KX
    Zhonghua Yan Ke Za Zhi; 2008 Jun; 44(6):529-33. PubMed ID: 19035245
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Mapping cerebellar abiotrophy in Australian Kelpies.
    Shearman JR; Cook RW; McCowan C; Fletcher JL; Taylor RM; Wilton AN
    Anim Genet; 2011 Dec; 42(6):675-8. PubMed ID: 22035013
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling.
    Arbour NC; Zlotogora J; Knowlton RG; Merin S; Rosenmann A; Kanis AB; Rokhlina T; Stone EM; Sheffield VC
    Hum Mol Genet; 1997 May; 6(5):689-94. PubMed ID: 9158143
    [TBL] [Abstract][Full Text] [Related]  

  • 98. An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4.
    Kahrizi K; Najmabadi H; Kariminejad R; Jamali P; Malekpour M; Garshasbi M; Ropers HH; Kuss AW; Tzschach A
    Eur J Hum Genet; 2009 Jan; 17(1):125-8. PubMed ID: 18781183
    [TBL] [Abstract][Full Text] [Related]  

  • 99. Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community.
    Farrer LA; Bowirrat A; Friedland RP; Waraska K; Korczyn AD; Baldwin CT
    Hum Mol Genet; 2003 Feb; 12(4):415-22. PubMed ID: 12566388
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.
    Lahat H; Eldar M; Levy-Nissenbaum E; Bahan T; Friedman E; Khoury A; Lorber A; Kastner DL; Goldman B; Pras E
    Circulation; 2001 Jun; 103(23):2822-7. PubMed ID: 11401939
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.