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 *

175 related articles for article (PubMed ID: 19419450)

  • 1. Genetic analysis of familial non-syndromic primary failure of eruption.
    Frazier-Bowers SA; Simmons D; Koehler K; Zhou J
    Orthod Craniofac Res; 2009 May; 12(2):74-81. PubMed ID: 19419450
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel mutations in PTH1R associated with primary failure of eruption and osteoarthritis.
    Frazier-Bowers SA; Hendricks HM; Wright JT; Lee J; Long K; Dibble CF; Bencharit S
    J Dent Res; 2014 Feb; 93(2):134-9. PubMed ID: 24300310
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exome resequencing combined with linkage analysis identifies novel PTH1R variants in primary failure of tooth eruption in Japanese.
    Yamaguchi T; Hosomichi K; Narita A; Shirota T; Tomoyasu Y; Maki K; Inoue I
    J Bone Miner Res; 2011 Jul; 26(7):1655-61. PubMed ID: 21404329
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Primary failure of eruption (PFE)--clinical and molecular genetics analysis.
    Stellzig-Eisenhauer A; Decker E; Meyer-Marcotty P; Rau C; Fiebig BS; Kress W; Saar K; Rüschendorf F; Hubner N; Grimm T; Witt E; Weber BH
    J Orofac Orthop; 2010 Jan; 71(1):6-16. PubMed ID: 20135246
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Primary failure of eruption and PTH1R: the importance of a genetic diagnosis for orthodontic treatment planning.
    Frazier-Bowers SA; Simmons D; Wright JT; Proffit WR; Ackerman JL
    Am J Orthod Dentofacial Orthop; 2010 Feb; 137(2):160.e1-7; discussion 160-1. PubMed ID: 20152661
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Primary failure of eruption (PFE). Clinical and molecular genetics analysis].
    Stellzig-Eisenhauer A; Decker E; Meyer-Marcotty P; Rau C; Fiebig BS; Kress W; Saar K; Rüschendorf F; Hubner N; Grimm T; Witt E; Weber BH
    Orthod Fr; 2013 Sep; 84(3):241-50. PubMed ID: 23993365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.
    Decker E; Stellzig-Eisenhauer A; Fiebig BS; Rau C; Kress W; Saar K; Rüschendorf F; Hubner N; Grimm T; Weber BH
    Am J Hum Genet; 2008 Dec; 83(6):781-6. PubMed ID: 19061984
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New locus for autosomal dominant high myopia maps to the long arm of chromosome 17.
    Paluru P; Ronan SM; Heon E; Devoto M; Wildenberg SC; Scavello G; Holleschau A; Mäkitie O; Cole WG; King RA; Young TL
    Invest Ophthalmol Vis Sci; 2003 May; 44(5):1830-6. PubMed ID: 12714612
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Autosomal dominant vasovagal syncope: clinical features and linkage to chromosome 15q26.
    Klein KM; Bromhead CJ; Smith KR; O'Callaghan CJ; Corcoran SJ; Heron SE; Iona X; Hodgson BL; McMahon JM; Lawrence KM; Scheffer IE; Dibbens LM; Bahlo M; Berkovic SF
    Neurology; 2013 Apr; 80(16):1485-93. PubMed ID: 23589636
    [TBL] [Abstract][Full Text] [Related]  

  • 10. KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption.
    Assiry AA; Albalawi AM; Zafar MS; Khan SD; Ullah A; Almatrafi A; Ramzan K; Basit S
    Sci Rep; 2019 Nov; 9(1):16469. PubMed ID: 31712638
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.
    Shugart YY; Silverberg MS; Duerr RH; Taylor KD; Wang MH; Zarfas K; Schumm LP; Bromfield G; Steinhart AH; Griffiths AM; Kane SV; Barmada MM; Rotter JI; Mei L; Bernstein CN; Bayless TM; Langelier D; Cohen A; Bitton A; Rioux JD; Cho JH; Brant SR
    Genes Immun; 2008 Mar; 9(2):161-7. PubMed ID: 18246054
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.
    Morlé L; Bozon M; Zech JC; Alloisio N; Raas-Rothschild A; Philippe C; Lambert JC; Godet J; Plauchu H; Edery P
    Am J Hum Genet; 2000 Dec; 67(6):1592-7. PubMed ID: 11035633
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23.
    Xu J; Zheng SL; Hawkins GA; Faith DA; Kelly B; Isaacs SD; Wiley KE; Chang B; Ewing CM; Bujnovszky P; Carpten JD; Bleecker ER; Walsh PC; Trent JM; Meyers DA; Isaacs WB
    Am J Hum Genet; 2001 Aug; 69(2):341-50. PubMed ID: 11443539
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic homogeneity for inherited congenital microcoria loci in an Asian Indian pedigree.
    Ramprasad VL; Sripriya S; Ronnie G; Nancarrow D; Saxena S; Hemamalini A; Kumar D; Vijaya L; Kumaramanickavel G
    Mol Vis; 2005 Nov; 11():934-40. PubMed ID: 16288197
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Establishing the diagnostic criteria for eruption disorders based on genetic and clinical data.
    Rhoads SG; Hendricks HM; Frazier-Bowers SA
    Am J Orthod Dentofacial Orthop; 2013 Aug; 144(2):194-202. PubMed ID: 23910200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Linkage of autosomal dominant common variable immunodeficiency to chromosome 5p and evidence for locus heterogeneity.
    Braig DU; Schäffer AA; Glocker E; Salzer U; Warnatz K; Peter HH; Grimbacher B
    Hum Genet; 2003 Apr; 112(4):369-78. PubMed ID: 12574940
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.
    Chen S; Ondo WG; Rao S; Li L; Chen Q; Wang Q
    Am J Hum Genet; 2004 May; 74(5):876-85. PubMed ID: 15077200
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A three-dimensional analysis of primary failure of eruption in humans and mice.
    Tokavanich N; Gupta A; Nagata M; Takahashi A; Matsushita Y; Yatabe M; Ruellas A; Cevidanes L; Maki K; Yamaguchi T; Ono N; Ono W
    Oral Dis; 2020 Mar; 26(2):391-400. PubMed ID: 31802584
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
    Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.