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 *

154 related articles for article (PubMed ID: 19266219)

  • 1. A locus for autosomal dominant reflex epilepsy precipitated by hot water maps at chromosome 10q21.3-q22.3.
    Ratnapriya R; Satishchandra P; Kumar SD; Gadre G; Reddy R; Anand A
    Hum Genet; 2009 Jun; 125(5-6):541-9. PubMed ID: 19266219
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial autosomal dominant reflex epilepsy triggered by hot water maps to 4q24-q28.
    Ratnapriya R; Satishchandra P; Dilip S; Gadre G; Anand A
    Hum Genet; 2009 Nov; 126(5):677-83. PubMed ID: 19597845
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A genetic locus for sensory epilepsy precipitated by contact with hot water maps to chromosome 9p24.3-p23.
    Karan KR; Satishchandra P; Sinha S; Anand A
    J Genet; 2018 Jun; 97(2):391-398. PubMed ID: 29932058
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani family.
    Malik S; Grzeschik KH
    Hum Genet; 2008 Mar; 123(2):197-205. PubMed ID: 18193458
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.
    Bowles KR; Gajarski R; Porter P; Goytia V; Bachinski L; Roberts R; Pignatelli R; Towbin JA
    J Clin Invest; 1996 Sep; 98(6):1355-60. PubMed ID: 8823300
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21.
    Volders PG; Zhu Q; Timmermans C; Eurlings PM; Su X; Arens YH; Li L; Jongbloed RJ; Xia M; Rodriguez LM; Chen YH
    Heart Rhythm; 2007 Apr; 4(4):469-75. PubMed ID: 17399636
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
    Hanein S; Dürr A; Ribai P; Forlani S; Leutenegger AL; Nelson I; Babron MC; Elleuch N; Depienne C; Charon C; Brice A; Stevanin G
    Hum Genet; 2007 Nov; 122(3-4):261-73. PubMed ID: 17605047
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a Novel Gene on 10q22.1 Causing Autosomal Dominant Retinitis Pigmentosa (adRP).
    Daiger SP; Sullivan LS; Bowne SJ; Koboldt DC; Blanton SH; Wheaton DK; Avery CE; Cadena ED; Koenekoop RK; Fulton RS; Wilson RK; Weinstock GM; Lewis RA; Birch DG
    Adv Exp Med Biol; 2016; 854():193-200. PubMed ID: 26427411
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new locus for congenital cataract, microcornea, microphthalmia, and atypical iris coloboma maps to chromosome 2.
    Abouzeid H; Meire FM; Osman I; ElShakankiri N; Bolay S; Munier FL; Schorderet DF
    Ophthalmology; 2009 Jan; 116(1):154-162.e1. PubMed ID: 19004499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new locus for dominant "zonular pulverulent" cataract, on chromosome 13.
    Mackay D; Ionides A; Berry V; Moore A; Bhattacharya S; Shiels A
    Am J Hum Genet; 1997 Jun; 60(6):1474-8. PubMed ID: 9199569
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.
    Lin Y; Liu T; Li J; Yang J; Du Q; Wang J; Yang Y; Liu X; Fan Y; Lu F; Chen Y; Pu Y; Zhang K; He X; Yang Z
    Mol Vis; 2008 Apr; 14():739-44. PubMed ID: 18432317
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33.
    Dai XH; Chen WW; Wang X; Zhu QH; Li C; Li L; Liu MG; Wang QK; Liu JY
    Hum Genet; 2008 Nov; 124(4):423-9. PubMed ID: 18830713
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22.
    Chaib H; Place C; Salem N; Dodé C; Chardenoux S; Weissenbach J; el Zir E; Loiselet J; Petit C
    Hum Mol Genet; 1996 Jul; 5(7):1061-4. PubMed ID: 8817348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant "cerulean cataract" in an Indian family.
    Vanita V; Singh D; Robinson PN; Sperling K; Singh JR
    Am J Med Genet A; 2006 Mar; 140(6):558-66. PubMed ID: 16470690
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11.
    Kinirons P; Verlaan DJ; Dubé MP; Poirier J; Deacon C; Lortie A; Clément JF; Desbiens R; Carmant L; Cieuta-Walti C; Shevell M; Rouleau GA; Cossette P
    Am J Med Genet A; 2008 Mar; 146A(5):578-84. PubMed ID: 18241056
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.
    Nallasamy S; Paluru PC; Devoto M; Wasserman NF; Zhou J; Young TL
    Mol Vis; 2007 Feb; 13():229-36. PubMed ID: 17327828
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.
    Ratnamala U; Lyle R; Rawal R; Singh R; Vishnupriya S; Himabindu P; Rao V; Aggarwal S; Paluru P; Bartoloni L; Young TL; Paoloni-Giacobino A; Morris MA; Nath SK; Antonarakis SE; Radhakrishna U
    Invest Ophthalmol Vis Sci; 2011 Aug; 52(9):6814-9. PubMed ID: 21357393
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The novel gene locus for agenesis of permanent teeth (He-Zhao deficiency) maps to chromosome 10q11.2.
    Liu W; Wang H; Zhao S; Zhao W; Bai S; Zhao Y; Xu S; Wu C; Huang W; Chen Z; Feng G; He L
    J Dent Res; 2001 Aug; 80(8):1716-20. PubMed ID: 11669481
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel form of "central pouchlike" cataract, with sutural opacities, maps to chromosome 15q21-22.
    Vanita ; Singh JR; Sarhadi VK; Singh D; Reis A; Rueschendorf F; Becker-Follmann J; Jung M; Sperling K
    Am J Hum Genet; 2001 Feb; 68(2):509-14. PubMed ID: 11133359
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An autosomal dominant posterior polar cataract locus maps to human chromosome 20p12-q12.
    Yamada K; Tomita H; Yoshiura K; Kondo S; Wakui K; Fukushima Y; Ikegawa S; Nakamura Y; Amemiya T; Niikawa N
    Eur J Hum Genet; 2000 Jul; 8(7):535-9. PubMed ID: 10909854
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.