These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 11519376)

  • 101. Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data.
    Jiang H; Orr A; Guernsey DL; Robitaille J; Asselin G; Samuels ME; Dubé MP
    PLoS One; 2009; 4(4):e5280. PubMed ID: 19399176
    [TBL] [Abstract][Full Text] [Related]  

  • 102. Homozygosity mapping of a Desbuquois dysplasia locus to chromosome 17q25.3.
    Faivre L; Le Merrer M; Al-Gazali LI; Ausems MG; Bitoun P; Bacq D; Maroteaux P; Munnich A; Cormier-Daire V
    J Med Genet; 2003 Apr; 40(4):282-4. PubMed ID: 12676900
    [TBL] [Abstract][Full Text] [Related]  

  • 103. An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.
    Fukushima K; Ramesh A; Srisailapathy CR; Ni L; Wayne S; O'Neill ME; Van Camp G; Coucke P; Jain P; Wilcox ER; Smith SD; Kenyon JB; Zbar RI; Smith RJ
    Genome Res; 1995 Oct; 5(3):305-8. PubMed ID: 8593615
    [TBL] [Abstract][Full Text] [Related]  

  • 104. A progeroid syndrome with neonatal presentation and long survival maps to 19p13.3p13.2.
    Akawi N; Ali B; Al Gazali L
    Birth Defects Res A Clin Mol Teratol; 2013 Jul; 97(7):456-62. PubMed ID: 23696134
    [TBL] [Abstract][Full Text] [Related]  

  • 105. Genetic analysis of cataract in Ihara epileptic rat.
    Yokoyama M; Amano S; Tsuji A; Sasahara M; Serikawa T; Ihara N; Matsuda M; Hazama F; Handa J
    Mamm Genome; 2001 Mar; 12(3):207-11. PubMed ID: 11252169
    [TBL] [Abstract][Full Text] [Related]  

  • 106. Mapping of Nakano cataract gene nct on mouse chromosome 16.
    Hiai H; Kato S; Horiuchi Y; Shimada R; Tsuruyama T; Watanabe T; Matsuzawa A
    Genomics; 1998 May; 50(1):119-20. PubMed ID: 9628833
    [No Abstract]   [Full Text] [Related]  

  • 107. A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.
    Shohat M; Lotan R; Magal N; Shohat T; Fischel-Ghodsian N; Rotter JI; Jaber L
    Am J Hum Genet; 1997 Nov; 61(5):1139-43. PubMed ID: 9345093
    [TBL] [Abstract][Full Text] [Related]  

  • 108. Assignment of the human cardiac/slow skeletal muscle troponin C gene (TNNC1) between D3S3118 and GCT4B10 on the short arm of chromosome 3 by somatic cell hybrid analysis.
    Townsend PJ; Yacoub MH; Barton PJ
    Ann Hum Genet; 1997 Jul; 61(Pt 4):375-7. PubMed ID: 9365790
    [TBL] [Abstract][Full Text] [Related]  

  • 109. A locus for Fanconi anemia on 16q determined by homozygosity mapping.
    Gschwend M; Levran O; Kruglyak L; Ranade K; Verlander PC; Shen S; Faure S; Weissenbach J; Altay C; Lander ES; Auerbach AD; Botstein D
    Am J Hum Genet; 1996 Aug; 59(2):377-84. PubMed ID: 8755924
    [TBL] [Abstract][Full Text] [Related]  

  • 110. Re-assigning the DFNB33 locus to chromosome 10p11.23-q21.1.
    Belguith H; Masmoudi S; Medlej-Hashim M; Chouery E; Weil D; Ayadi H; Petit C; Mégarbané A
    Eur J Hum Genet; 2009 Jan; 17(1):122-4. PubMed ID: 18781188
    [TBL] [Abstract][Full Text] [Related]  

  • 111. Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.
    Ali G; Lee K; Andrade PB; Basit S; Santos-Cortez RL; Chen L; Jelani M; Ansar M; Ahmad W; Leal SM
    Hum Hered; 2011; 71(2):106-12. PubMed ID: 21734401
    [TBL] [Abstract][Full Text] [Related]  

  • 112. Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies.
    Aksentijevich I; Pras E; Gruberg L; Shen Y; Holman K; Helling S; Prosen L; Sutherland GR; Richards RI; Ramsburg M
    Am J Hum Genet; 1993 Aug; 53(2):451-61. PubMed ID: 8328461
    [TBL] [Abstract][Full Text] [Related]  

  • 113. A G-to-A single nucleotide polymorphism in the human alpha 2 delta 2 calcium channel subunit gene that maps at chromosome 3p21.3.
    Angeloni D; Wei MH; Duh FM; Johnson BE; Lerman MI
    Mol Cell Probes; 2000 Feb; 14(1):53-4. PubMed ID: 10722793
    [No Abstract]   [Full Text] [Related]  

  • 114. A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32.
    Hattersley K; Laurie KJ; Liebelt JE; Gecz J; Durkin SR; Craig JE; Burdon KP
    BMC Med Genet; 2010 Nov; 11():165. PubMed ID: 21092079
    [TBL] [Abstract][Full Text] [Related]  

  • 115. A novel gene for neonatal diabetes maps to chromosome 10p12.1-p13.
    Sellick GS; Garrett C; Houlston RS
    Diabetes; 2003 Oct; 52(10):2636-8. PubMed ID: 14514650
    [TBL] [Abstract][Full Text] [Related]  

  • 116. Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis.
    Samples JR; Kitsos G; Economou-Petersen E; Steinkamp P; Sykes R; Rust K; Patzer C; Grigoriadou M; Aperis G; Psilas K; Petersen MB; Wirtz MK
    Clin Genet; 2004 Jan; 65(1):40-4. PubMed ID: 15032973
    [TBL] [Abstract][Full Text] [Related]  

  • 117. The hereditary pancreatitis gene maps to long arm of chromosome 7.
    Le Bodic L; Bignon JD; Raguénès O; Mercier B; Georgelin T; Schnee M; Soulard F; Gagne K; Bonneville F; Muller JY; Bachner L; Férec C
    Hum Mol Genet; 1996 Apr; 5(4):549-54. PubMed ID: 8845851
    [TBL] [Abstract][Full Text] [Related]  

  • 118. Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy.
    Zara F; Labuda M; Garofalo PG; Durisotti C; Bianchi A; Castellotti B; Patel PI; Avanzini G; Pandolfo M
    Neurology; 1998 Aug; 51(2):493-8. PubMed ID: 9710024
    [TBL] [Abstract][Full Text] [Related]  

  • 119. A minimalist approach to gene mapping: locating the gene for acheiropodia, by homozygosity analysis.
    Escamilla MA; DeMille MC; Benavides E; Roche E; Almasy L; Pittman S; Hauser J; Lew DF; Freimer NB; Whittle MR
    Am J Hum Genet; 2000 Jun; 66(6):1995-2000. PubMed ID: 10780921
    [TBL] [Abstract][Full Text] [Related]  

  • 120. Gene locus ambiguity in posterior urethral valves/prune-belly syndrome.
    Weber S; Mir S; Schlingmann KP; Nürnberg G; Becker C; Kara PE; Ozkayin N; Konrad M; Nürnberg P; Schaefer F
    Pediatr Nephrol; 2005 Aug; 20(8):1036-42. PubMed ID: 15912376
    [TBL] [Abstract][Full Text] [Related]  

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