BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 9475589)

  • 1. Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classification.
    Robin NH; Scott JA; Arnold JE; Goldstein JA; Shilling BB; Marion RW; Cohen MM
    Am J Med Genet; 1998 Jan; 75(3):240-4. PubMed ID: 9475589
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pfeiffer syndrome.
    Vogels A; Fryns JP
    Orphanet J Rare Dis; 2006 Jun; 1():19. PubMed ID: 16740155
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversion.
    Oliveira NA; Alonso LG; Fanganiello RD; Passos-Bueno MR
    Birth Defects Res A Clin Mol Teratol; 2006 Aug; 76(8):629-33. PubMed ID: 16955501
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FGFR1 and FGFR2 mutations in Pfeiffer syndrome.
    Chokdeemboon C; Mahatumarat C; Rojvachiranonda N; Tongkobpetch S; Suphapeetiporn K; Shotelersuk V
    J Craniofac Surg; 2013 Jan; 24(1):150-2. PubMed ID: 23348274
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pfeiffer syndrome type 2: further delineation and review of the literature.
    Plomp AS; Hamel BC; Cobben JM; Verloes A; Offermans JP; Lajeunie E; Fryns JP; de Die-Smulders CE
    Am J Med Genet; 1998 Jan; 75(3):245-51. PubMed ID: 9475590
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Intestinal malrotation in a patient with Pfeiffer syndrome type 2.
    Zarate YA; Putnam PE; Saal HM
    Cleft Palate Craniofac J; 2010 Nov; 47(6):638-41. PubMed ID: 20509766
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Type V acrocephalosyndactylia (Pfeiffer's syndrome). Apropos of 3 cases in the same family].
    Manouvrier-Hanu S; Herbaux B; Pellerin P; Douchet P; Bouchez-Bonniere MC; Dubos JP; Farriaux JP
    Arch Fr Pediatr; 1989; 46(6):433-7. PubMed ID: 2783004
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of type 2 Pfeiffer syndrome.
    Bernstein PS; Gross SJ; Cohen DJ; Tiller GR; Shanske AL; Bombard AT; Marion RW
    Ultrasound Obstet Gynecol; 1996 Dec; 8(6):425-8. PubMed ID: 9014285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature.
    Nazzaro A; Della Monica M; Lonardo F; Di Blasi A; Baffico M; Baldi M; Nazzaro G; De Placido G; Scarano G
    Prenat Diagn; 2004 Nov; 24(11):918-22. PubMed ID: 15565658
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Tracheal anomalies in Pfeiffer syndrome.
    Hockstein NG; McDonald-McGinn D; Zackai E; Bartlett S; Huff DS; Jacobs IN
    Arch Otolaryngol Head Neck Surg; 2004 Nov; 130(11):1298-302. PubMed ID: 15545585
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pfeiffer syndrome: analysis of a clinical series and development of a classification system.
    Greig AV; Wagner J; Warren SM; Grayson B; McCarthy JG
    J Craniofac Surg; 2013 Jan; 24(1):204-15. PubMed ID: 23348287
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pfeiffer Syndrome type 2--case report.
    Oyamada MK; Ferreira HS; Hoff M
    Sao Paulo Med J; 2003 Jul; 121(4):176-9. PubMed ID: 14595512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pfeiffer syndrome: a clinical review.
    Moore MH; Cantrell SB; Trott JA; David DJ
    Cleft Palate Craniofac J; 1995 Jan; 32(1):62-70. PubMed ID: 7727489
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review.
    Peña-Padilla C; Viramontes-Aguilar L; Tavares-Macías G; Bobadilla-Morales L; L Cunningham M; Park S; Zapata-Aldana E; Corona-Rivera JR
    Fetal Pediatr Pathol; 2019 Oct; 38(5):412-417. PubMed ID: 31002276
    [No Abstract]   [Full Text] [Related]  

  • 15. [Syndromes 2. Pfeiffer syndrome].
    Freihofer HP
    Ned Tijdschr Tandheelkd; 1998 Jul; 105(7):245-6. PubMed ID: 11928428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pfeiffer syndrome: clinical and genetic findings in five Brazilian families.
    Júnior HM; de Aquino SN; Machado RA; Leão LL; Coletta RD; Burle-Aguiar MJ
    Med Oral Patol Oral Cir Bucal; 2015 Jan; 20(1):e52-8. PubMed ID: 25129254
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pfeiffer syndrome: systemic and ocular implications.
    Harb E; Kran B
    Optometry; 2005 Jul; 76(7):352-62. PubMed ID: 16038862
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical expression in Pfeiffer syndrome type 2 and 3: surveillance in Japan.
    Koga H; Suga N; Nakamoto T; Tanaka K; Takahashi N
    Am J Med Genet A; 2012 Oct; 158A(10):2506-10. PubMed ID: 22965899
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial arthropathy in Saudi Arabian children: demographic, clinical, and biochemical features.
    Al-Mayouf SM
    Semin Arthritis Rheum; 2007 Feb; 36(4):256-61. PubMed ID: 16996580
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pfeiffer syndrome: an unusual type of acrocephalosyndactyl with broad thumbs and great toes.
    Cracco J; Martzolf J; Carpenter GG; Jackson L; O'Hara AE
    Neurology; 1970 Apr; 20(4):414. PubMed ID: 5535071
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.