BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 957376)

  • 21. The feet in Pfeiffer's syndrome.
    Anderson PJ; Hall CM; Evans RD; Jones BM; Hayward RD
    J Craniofac Surg; 1998 Jan; 9(1):83-7. PubMed ID: 9558574
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case of Pfeiffer syndrome.
    Park MS; Yoo JE; Chung J; Yoon SH
    J Korean Med Sci; 2006 Apr; 21(2):374-8. PubMed ID: 16614535
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Variable expressivity of pfeiffer syndrome in a family with FGFR1 p.Pro252Arg mutation.
    Bessenyei B; Tihanyi M; Hartwig M; Szakszon K; Oláh É
    Am J Med Genet A; 2014 Dec; 164A(12):3176-9. PubMed ID: 25251565
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome?
    Preis S; Kaewel EV; Majewski F
    Clin Genet; 1995 May; 47(5):267-9. PubMed ID: 7554354
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [A dominant syndrome associated with polysyndactyly, spatule thumb, facial abnormalities, and mental retardation. (A particular form of Noack's acrocephalosyndactylia)].
    Gnamey D; Farriaux JP
    J Genet Hum; 1971 Dec; 19(4):299-316. PubMed ID: 5152131
    [No Abstract]   [Full Text] [Related]  

  • 26. A family with the Saethre-Chotzen syndrome.
    Bianchi E; Aricŏ M; Podestă AF; Grana M; Fiori P; Beluffi G
    Am J Med Genet; 1985 Dec; 22(4):649-58. PubMed ID: 4073118
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Oto-palato-digital syndrome. Clinico-radiological study].
    Beluffi G; Pazzaglia UE; Fiori P; Pricca P; Poznanski AK
    Radiol Med; 1987 Sep; 74(3):176-84. PubMed ID: 3659425
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Heart-hand syndrome. III. A new syndrome in three generations.
    Ruiz de la Fuente S; Prieto F
    Hum Genet; 1980; 55(1):43-7. PubMed ID: 7450756
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. A distinct autosomal dominant craniosynostosis-brachydactyly syndrome.
    Glass IA; Chapman S; Hockley AD
    Clin Dysmorphol; 1994 Jul; 3(3):215-23. PubMed ID: 7981856
    [TBL] [Abstract][Full Text] [Related]  

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

  • 32. Apert syndrome.
    Suparta N; Hartono ; Sunartini
    Paediatr Indones; 1991; 31(11-12):319-24. PubMed ID: 1845657
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Acrocephalosyndactyly I (Apert syndrome)].
    Linss G
    Hautarzt; 2000 Sep; 51(9):685-7. PubMed ID: 11057397
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Brachydactyly type E in two sibs with increased bone density and mental retardation. A new autosomal recessive syndrome?
    Stoll C; Alembik Y
    Genet Couns; 2004; 15(4):421-8. PubMed ID: 15658617
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Anorectal anomaly in Pfeiffer syndrome.
    Ohashi H; Nishimoto H; Nishimura J; Sato M; Imaizumi S; Aihara T; Fukushima Y
    Clin Dysmorphol; 1993 Jan; 2(1):28-33. PubMed ID: 8298735
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Brachydactyly type A4 (brachymesophalangia II and V, Temtamy type). A rare type of brachydactyly].
    Reichenbach H; Hörmann D; Theile H
    Kinderarztl Prax; 1993 Mar; 61(2):59-62. PubMed ID: 8510402
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hyperphalangism accompanied by brachydactyly of the feet: a case report.
    Suresh SS; Abraham R
    Acta Orthop Traumatol Turc; 2010; 44(1):79-81. PubMed ID: 20513996
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 7.