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 *

138 related articles for article (PubMed ID: 7594749)

  • 1. Perspectives on craniofacial asymmetry. V. The craniosynostoses.
    Cohen MM
    Int J Oral Maxillofac Surg; 1995 Jun; 24(3):191-4. PubMed ID: 7594749
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Saethre-Chotzen syndrome: review of the literature and report of a case.
    Clauser L; Galiè M; Hassanipour A; Calabrese O
    J Craniofac Surg; 2000 Sep; 11(5):480-6. PubMed ID: 11314068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Monozygotic twins with Apert syndrome.
    Breugem CC; Fitzpatrick DF; Verchere C
    Cleft Palate Craniofac J; 2008 Jan; 45(1):101-4. PubMed ID: 18215098
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phenotypic variation in acrocephalosyndactyly syndromes: unusual findings in patient with features of Apert and Saethre-Chotzen syndromes.
    Cantrell SB; Moore MH; Trott JA; Morris RJ; David DJ
    Cleft Palate Craniofac J; 1994 Nov; 31(6):487-93. PubMed ID: 7833342
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Automated three-dimensional analysis of facial asymmetry in patients with syndromic coronal synostosis: A retrospective study.
    Choi TM; Liu X; Abdel-Alim T; van Veelen ML; Mathijssen IMJ; Wolvius EB; Roshchupkin GV
    J Craniomaxillofac Surg; 2024 Jan; 52(1):48-54. PubMed ID: 38135649
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7p.
    von Gernet S; Schuffenhauer S; Golla A; Lichtner P; Balg S; Mühlbauer W; Murken J; Fairley J; Meitinger T
    Am J Med Genet; 1996 May; 63(1):177-84. PubMed ID: 8723106
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Syndromes involving craniosynostosis and midface hypoplasia.
    Katzen JT; McCarthy JG
    Otolaryngol Clin North Am; 2000 Dec; 33(6):1257-84, vi. PubMed ID: 11449786
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
    Sharma VP; Fenwick AL; Brockop MS; McGowan SJ; Goos JA; Hoogeboom AJ; Brady AF; Jeelani NO; Lynch SA; Mulliken JB; Murray DJ; Phipps JM; Sweeney E; Tomkins SE; Wilson LC; Bennett S; Cornall RJ; Broxholme J; Kanapin A; ; Johnson D; Wall SA; van der Spek PJ; Mathijssen IM; Maxson RE; Twigg SR; Wilkie AO
    Nat Genet; 2013 Mar; 45(3):304-7. PubMed ID: 23354436
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Saethre-Chotzen syndrome: a case report].
    Díez de Los Ríos Quintanero B; Gracia Rojas E; Ortiz Movilla R; Cabrejas Núñez MJ; Marín Gabriel MÁ
    Arch Argent Pediatr; 2021 Apr; 119(2):e129-e132. PubMed ID: 33749202
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Facial malformations and spinal anomalies. A predictable relationship.
    Sherk HH; Whitaker LA; Pasquariello PS
    Spine (Phila Pa 1976); 1982; 7(6):526-31. PubMed ID: 7167823
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Postnatal onset of craniosynostosis in a case of Saethre-Chotzen syndrome.
    de Heer IM; Hoogeboom J; Vermeij-Keers C; de Klein A; Vaandrager JM
    J Craniofac Surg; 2004 Nov; 15(6):1048-52. PubMed ID: 15547403
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome.
    Teng CS; Ting MC; Farmer DT; Brockop M; Maxson RE; Crump JG
    Elife; 2018 Oct; 7():. PubMed ID: 30375332
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The genetic background of craniosynostosis syndromes.
    Heutink P; Vermeij-Keers C; Oostra BA
    Eur J Hum Genet; 1995; 3(5):312-23. PubMed ID: 8556306
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2.
    Reardon W; McManus SP; Summers D; Winter RM
    Am J Med Genet; 1993 Oct; 47(5):633-6. PubMed ID: 8266988
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Morphology of the foramen magnum in syndromic and non-syndromic brachycephaly.
    Assadsangabi R; Hajmomenian M; Bilaniuk LT; Vossough A
    Childs Nerv Syst; 2015 May; 31(5):735-41. PubMed ID: 25686894
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Progressive facial asymmetry as a result of early closure of the left coronal suture.
    Arvystas MG; Antonellis P; Justin AF
    Am J Orthod; 1985 Mar; 87(3):240-6. PubMed ID: 3856397
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Y-craniosynostosis by premature fusion of the metopic and coronal sutures: a new nosological entity or a variety of Saethre-Chotzen syndrome?
    di Rocco F; Benoit A; Vigneron J; Segura PB; Klein O; Collet C; Arnaud E
    Birth Defects Res A Clin Mol Teratol; 2015 Apr; 103(4):306-10. PubMed ID: 25808521
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Genetic causes of syndromic craniosynostoses.
    Jezela-Stanek A; Krajewska-Walasek M
    Eur J Paediatr Neurol; 2013 May; 17(3):221-4. PubMed ID: 23062756
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Upper facial asymmetries resulting from unilateral coronal synostosis. Diagnosis and surgical reconstruction.
    Posnick JC
    Atlas Oral Maxillofac Surg Clin North Am; 1996 Mar; 4(1):53-66. PubMed ID: 11878266
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.