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 *

120 related articles for article (PubMed ID: 20129888)

  • 1. Robinow syndrome, Cockayne syndrome, and Pfeiffer syndrome: an overview of physical, neurological, and oral characteristics.
    Horbelt CV
    Gen Dent; 2010; 58(1):14-7. PubMed ID: 20129888
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical manifestations of terminal osseous dysplasia and pigmentary defects in a young girl.
    Lin BP; Lin MI; Berlocher WC
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2003 May; 95(5):607-13. PubMed ID: 12738953
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Craniofacial bony defect with developmental abnormality of facial bones, dental malalignment and ectopic neural tissue in the internal auditory meati--a new syndrome?
    Colleran GC; Hayes R; Kearns G; Kavanagh P; Moylett E; Lynch SA
    Eur J Med Genet; 2014; 57(6):302-5. PubMed ID: 24705061
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Orofacial manifestations of Robinow's syndrome: a case report in a pediatric patient.
    Cerqueira DF; de Souza IP
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Mar; 105(3):353-7. PubMed ID: 18061493
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Knobloch syndrome: novel intra-oral findings.
    O'Connell AC; Toner M; Murphy S
    Int J Paediatr Dent; 2009 May; 19(3):213-5. PubMed ID: 18445000
    [No Abstract]   [Full Text] [Related]  

  • 6. Autosomal recessive Robinow syndrome: a case report.
    Grothe R; Anderson-Cermin C; Beiraghi S
    J Dent Child (Chic); 2008; 75(1):48-54. PubMed ID: 18505648
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cerebro-osseous-digital syndrome: four new cases of a lethal skeletal dysplasia--distinct from Neu-Laxova Syndrome.
    Elliott AM; Gonzales M; Hoeffel JC; Le Merrer M; Maroteaux P; Encha-Razavi F; Joye N; Berchel C; Fliegel C; Aughton DJ; Beaudry-Rodgers K; Hasteh F; Nerlich AG; Wilcox WR; Rimoin DL; Lachman RS; Freisinger P
    Am J Med Genet; 2002 Apr; 109(2):139-48. PubMed ID: 11977163
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A possible cranio-oro-facial phenotype in Cockayne syndrome.
    Bloch-Zupan A; Rousseaux M; Laugel V; Schmittbuhl M; Mathis R; Desforges E; Koob M; Zaloszyc A; Dollfus H; Laugel V
    Orphanet J Rare Dis; 2013 Jan; 8():9. PubMed ID: 23311583
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel dental anomalies associated with congenital contractural arachnodactyly: a case report.
    Ayers KM; Drummond BK
    Pediatr Dent; 2003; 25(5):501-4. PubMed ID: 14649616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Russell-Silver syndrome: a study of 3 cases.
    Kulkarni ML; Venkataramana V; Sureshkumar C; Shabeer HM
    Ann Dent; 1995; 54(1-2):56-60. PubMed ID: 8572550
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Neonatal death in Marshall-Smith syndrome.
    Chatel C; Maazoul F; Sigaudy S; Fredouille C; Ayme S; Philip N
    Genet Couns; 1998; 9(1):15-8. PubMed ID: 9555581
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The oral manifestations of Apert syndrome.
    Kreiborg S; Cohen MM
    J Craniofac Genet Dev Biol; 1992; 12(1):41-8. PubMed ID: 1572940
    [TBL] [Abstract][Full Text] [Related]  

  • 13. KBG syndrome: review of the literature and findings of 5 affected patients.
    Kumar H; Prabhu N; Cameron A
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 Sep; 108(3):e72-9. PubMed ID: 19716495
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Apert syndrome: a case report with discussion of craniofacial features.
    Paravatty RP; Ahsan A; Sebastian BT; Pai KM; Dayal PK
    Quintessence Int; 1999 Jun; 30(6):423-6. PubMed ID: 10635279
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Oral and craniofacial morphology of a patient with Larsen syndrome.
    Tsang MC; Ling JY; King NM; Chow SK
    J Craniofac Genet Dev Biol; 1986; 6(4):357-62. PubMed ID: 3793859
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Siblings with neonatal progeroid syndrome (Wiedemann-Rautenstrauch)].
    Hoppen T; Naumann A; Theile U; Rister M
    Klin Padiatr; 2004; 216(2):70-1. PubMed ID: 15106077
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Craniofacial and intraoral phenotype of Robinow syndrome forms.
    Beiraghi S; Leon-Salazar V; Larson BE; John MT; Cunningham ML; Petryk A; Lohr JL
    Clin Genet; 2011 Jul; 80(1):15-24. PubMed ID: 21496006
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement.
    Bailleul-Forestier I; Berdal A; Vinckier F; de Ravel T; Fryns JP; Verloes A
    Eur J Med Genet; 2008; 51(5):383-408. PubMed ID: 18599376
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dental findings in Kabuki make-up syndrome: a case report.
    Rocha CT; Peixoto IT; Fernandes PM; Torres CP; de Queiroz AM
    Spec Care Dentist; 2008; 28(2):53-7. PubMed ID: 18402617
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Report of a new syndrome: focus on differential diagnosis and review of Ellis-van Creveld, Curry-Hall, acrofacial dysostosis, and orofacial digital syndromes.
    Ghosh S; Setty S; Sivakumar A; Pai KM
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2007 May; 103(5):670-6. PubMed ID: 17466885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.