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 *

182 related articles for article (PubMed ID: 12938037)

  • 1. Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12).
    Sutton VR; McAlister WH; Bertin TK; Kaffe S; Wang JC; Yano S; Shaffer LG; Lee B; Epstein CJ; Villar AJ
    Hum Genet; 2003 Oct; 113(5):447-51. PubMed ID: 12938037
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Paternal uniparental disomy of chromosome 14: confirmation of a clinically-recognizable phenotype.
    Stevenson DA; Brothman AR; Chen Z; Bayrak-Toydemir P; Longo N
    Am J Med Genet A; 2004 Sep; 130A(1):88-91. PubMed ID: 15368501
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Radiological evaluation of dysmorphic thorax of paternal uniparental disomy 14.
    Miyazaki O; Nishimura G; Kagami M; Ogata T
    Pediatr Radiol; 2011 Aug; 41(8):1013-9. PubMed ID: 21607596
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype.
    Chu C; Schwartz S; McPherson E
    Am J Med Genet A; 2004 Jun; 127A(2):167-71. PubMed ID: 15108205
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prenatal diagnostic indicators of paternal uniparental disomy 14.
    Curtis L; Antonelli E; Vial Y; Rimensberger P; Le Merrer M; Hinard C; Bottani A; Fokstuen S
    Prenat Diagn; 2006 Aug; 26(8):662-6. PubMed ID: 16715538
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prenatal findings and epimutations for paternal uniparental disomy for chromosome 14 syndrome.
    Watanabe T; Go H; Kagami M; Yasuda S; Nomura Y; Fujimori K
    J Obstet Gynaecol Res; 2015 Jul; 41(7):1133-6. PubMed ID: 25656753
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comprehensive clinical studies in 34 patients with molecularly defined UPD(14)pat and related conditions (Kagami-Ogata syndrome).
    Kagami M; Kurosawa K; Miyazaki O; Ishino F; Matsuoka K; Ogata T
    Eur J Hum Genet; 2015 Nov; 23(11):1488-98. PubMed ID: 25689926
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular mechanisms regulating phenotypic outcome in paternal and maternal uniparental disomy for chromosome 14.
    Ogata T; Kagami M; Ferguson-Smith AC
    Epigenetics; 2008; 3(4):181-7. PubMed ID: 18698157
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [When should evoke prenatal paternal uniparental disomy 14?].
    Boiffard F; Bénéteau C; Quéré MP; Philippe HJ; Le Vaillant C
    Gynecol Obstet Fertil; 2014 Apr; 42(4):254-7. PubMed ID: 24394322
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Segmental and full paternal isodisomy for chromosome 14 in three patients: narrowing the critical region and implication for the clinical features.
    Kagami M; Nishimura G; Okuyama T; Hayashidani M; Takeuchi T; Tanaka S; Ishino F; Kurosawa K; Ogata T
    Am J Med Genet A; 2005 Oct; 138A(2):127-32. PubMed ID: 16152632
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report.
    Chen CL; Lee CN; Lin MW; Hsu WW; Tai YY; Lin SY
    J Formos Med Assoc; 2019 Mar; 118(3):739-742. PubMed ID: 30616993
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Coat hanger appearances of the ribs: a useful diagnostic marker of paternal uniparental disomy of chromosome 14.
    Naik S; Temple IK
    Arch Dis Child; 2010 Nov; 95(11):909. PubMed ID: 20656731
    [No Abstract]   [Full Text] [Related]  

  • 13. Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion.
    Tsukishiro S; Li QY; Tanemura M; Sugiura-Ogasawara M; Suzumori K; Sonta SI
    J Hum Genet; 2005; 50(3):112-117. PubMed ID: 15747166
    [TBL] [Abstract][Full Text] [Related]  

  • 14. High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B.
    Colson C; Decamp M; Gruchy N; Coudray N; Ballandonne C; Bracquemart C; Molin A; Mittre H; Takatani R; Jüppner H; Kottler ML; Richard N
    Bone; 2019 Jun; 123():145-152. PubMed ID: 30905746
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Paternal uniparental disomy 14: introducing the "coat-hanger" sign.
    Offiah AC; Cornette L; Hall CM
    Pediatr Radiol; 2003 Jul; 33(7):509-12. PubMed ID: 12712270
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kagami-Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region.
    Ogata T; Kagami M
    J Hum Genet; 2016 Feb; 61(2):87-94. PubMed ID: 26377239
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Paternal UPD14 is responsible for a distinctive malformation complex.
    Kurosawa K; Sasaki H; Sato Y; Yamanaka M; Shimizu M; Ito Y; Okuyama T; Matsuo M; Imaizumi K; Kuroki Y; Nishimura G
    Am J Med Genet; 2002 Jul; 110(3):268-72. PubMed ID: 12116236
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Male Case of Kagami-Ogata Syndrome Caused by Paternal Unipaternal Disomy 14 as a Result of a Robertsonian Translocation.
    Wang X; Pang H; Shah BA; Gu H; Zhang L; Wang H
    Front Pediatr; 2020; 8():88. PubMed ID: 32211354
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of mouse conceptuses with uniparental duplication/deficiency for distal chromosome 12: comparison with chromosome 12 uniparental disomy and implications for genomic imprinting.
    Tevendale M; Watkins M; Rasberry C; Cattanach B; Ferguson-Smith AC
    Cytogenet Genome Res; 2006; 113(1-4):215-22. PubMed ID: 16575183
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hepatoblastoma in an infant with paternal uniparental disomy 14.
    Horii M; Horiuchi H; Momoeda M; Nakagawa M; Hirata M; Kusakawa I; Yamanaka M
    Congenit Anom (Kyoto); 2012 Dec; 52(4):219-20. PubMed ID: 23181499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.