BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 27228464)

  • 1. Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.
    Wenger TL; Dahl J; Bhoj EJ; Rosen A; McDonald-McGinn D; Zackai E; Jacobs I; Heike CL; Hing A; Santani A; Inglis AF; Sie KC; Cunningham M; Perkins J
    Genet Med; 2017 Jan; 19(1):62-68. PubMed ID: 27228464
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves.
    Noble AR; Cunningham ML; Lam A; Wenger TL; Sie KC; Perkins JA; Dahl JP
    Laryngoscope; 2022 Jan; 132(1):215-221. PubMed ID: 34133757
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and genetic characteristics of craniosynostosis in Hungary.
    Bessenyei B; Nagy A; Szakszon K; Mokánszki A; Balogh E; Ujfalusi A; Tihanyi M; Novák L; Bognár L; Oláh É
    Am J Med Genet A; 2015 Dec; 167A(12):2985-91. PubMed ID: 26289989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice.
    Lam AS; Liu CC; Deutsch GH; Rivera J; Perkins JA; Holmes G; Jabs EW; Cunningham ML; Dahl JP
    Laryngoscope; 2021 Apr; 131(4):E1349-E1356. PubMed ID: 32886384
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patients.
    Roscioli T; Elakis G; Cox TC; Moon DJ; Venselaar H; Turner AM; Le T; Hackett E; Haan E; Colley A; Mowat D; Worgan L; Kirk EP; Sachdev R; Thompson E; Gabbett M; McGaughran J; Gibson K; Gattas M; Freckmann ML; Dixon J; Hoefsloot L; Field M; Hackett A; Kamien B; Edwards M; Adès LC; Collins FA; Wilson MJ; Savarirayan R; Tan TY; Amor DJ; McGillivray G; White SM; Glass IA; David DJ; Anderson PJ; Gianoutsos M; Buckley MF
    Am J Med Genet C Semin Med Genet; 2013 Nov; 163C(4):259-70. PubMed ID: 24127277
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.
    Paumard-Hernández B; Berges-Soria J; Barroso E; Rivera-Pedroza CI; Pérez-Carrizosa V; Benito-Sanz S; López-Messa E; Santos F; García-Recuero II; Romance A; Ballesta-Martínez JM; López-González V; Campos-Barros Á; Cruz J; Guillén-Navarro E; Sánchez Del Pozo J; Lapunzina P; García-Miñaur S; Heath KE
    Eur J Hum Genet; 2015 Jul; 23(7):907-14. PubMed ID: 25271085
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Less common underlying genetic diagnoses found in a cohort of 139 individuals surgically corrected for craniosynostosis.
    Ittleman BR; Mckissick J; Bosanko KA; Ocal E; Golinko M; Zarate YA
    Am J Med Genet A; 2018 Feb; 176(2):487-491. PubMed ID: 29160013
    [No Abstract]   [Full Text] [Related]  

  • 8. Novel mutation detection in craniosynostosis promotes characterization, identification, gene expression, tissue engineering and helps clinical practice and translational research.
    Barik M; Bano R; Bajpai M; Tripathy M; Das S; Dwivedi S
    Neurol India; 2020; 68(2):435-439. PubMed ID: 32415020
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Roles of FGFR2 and twist in human craniosynostosis: insights from genetic mutations in cranial osteoblasts.
    Marie PJ; Kaabeche K; Guenou H
    Front Oral Biol; 2008; 12():144-159. PubMed ID: 18391499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations.
    Ko JM; Jeong SY; Yang JA; Park DH; Yoon SH
    Plast Reconstr Surg; 2012 May; 129(5):814e-821e. PubMed ID: 22544111
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tracheal Cartilaginous Sleeve in Syndromic Craniosynostosis: An Underrecognized Source of Significant Morbidity and Mortality.
    Pickrell BB; Meaike JD; Cañadas KT; Chandy BM; Buchanan EP
    J Craniofac Surg; 2017 May; 28(3):696-699. PubMed ID: 28468151
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve.
    Wenger TL; Bhoj EJ; Wetmore RF; Mennuti MT; Bartlett SP; Mollen TJ; McDonald-McGinn DM; Zackai EH
    Am J Med Genet A; 2015 Apr; 167A(4):852-7. PubMed ID: 25706251
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Clinical and genetic characteristics of craniosynostosis].
    Bessenyei B; Oláh E
    Orv Hetil; 2014 Mar; 155(9):341-7. PubMed ID: 24566698
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutation analysis of FGFR1-3 in 11 Japanese patients with syndromic craniosynostoses.
    Ohishi A; Nishimura G; Kato F; Ono H; Maruwaka K; Ago M; Suzumura H; Hirose E; Uchida Y; Fukami M; Ogata T
    Am J Med Genet A; 2017 Jan; 173(1):157-162. PubMed ID: 27683237
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical study and some molecular features of Mexican patients with syndromic craniosynostosis.
    Ibarra-Arce A; Almaraz-Salinas M; Martínez-Rosas V; Ortiz de Zárate-Alarcón G; Flores-Peña L; Romero-Valdovinos M; Olivo-Díaz A
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1266. PubMed ID: 32510873
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Craniosynostosis.
    Johnson D; Wilkie AO
    Eur J Hum Genet; 2011 Apr; 19(4):369-76. PubMed ID: 21248745
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Severe craniosynostosis in an infant with deletion 22q11.2 syndrome.
    Al-Hertani W; Hastings VA; McGowan-Jordan J; Hurteau J; Graham GE
    Am J Med Genet A; 2013 Jan; 161A(1):153-7. PubMed ID: 23239640
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NGS targeted screening of 100 Scandinavian patients with coronal synostosis.
    Topa A; Rohlin A; Andersson MK; Fehr A; Lovmar L; Stenman G; Kölby L
    Am J Med Genet A; 2020 Feb; 182(2):348-356. PubMed ID: 31837199
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosis.
    Stenirri S; Restagno G; Ferrero GB; Alaimo G; Sbaiz L; Mari C; Genitori L; Maurizio F; Cremonesi L
    Clin Chem; 2007 Oct; 53(10):1767-74. PubMed ID: 17693524
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Syndromic craniosynostosis, fibroblast growth factor receptor 2 (FGFR2) mutations, and sacrococcygeal eversion presenting as human tails.
    Wilkinson CC; Manchester DK; Keating RF; Ketch LL; Winston KR
    Childs Nerv Syst; 2012 Aug; 28(8):1221-6. PubMed ID: 22661218
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.