BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 2635655)

  • 1. [2 familial cases of cranio-metaphyseal dysostosis].
    Felli L; Giliberti R; Barneschi G
    Chir Organi Mov; 1989; 74(3-4):137-41. PubMed ID: 2635655
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new familial syndrome with craniofacial abnormalities, osseous defects and mental retardation.
    Grix A; Blankenship W; Peterson R; Hall B
    Birth Defects Orig Artic Ser; 1975; 11(5):107-14. PubMed ID: 1218201
    [No Abstract]   [Full Text] [Related]  

  • 3. Cranio-carpo-tarsal dysplasia. A report of seven cases.
    O'Connell DJ; Hall CM
    Radiology; 1977 Jun; 123(3):719-22. PubMed ID: 860039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Acromelic frontonasal dysostosis.
    Slaney SF; Goodman FR; Eilers-Walsman BL; Hall BD; Williams DK; Young ID; Hayward RD; Jones BM; Christianson AL; Winter RM
    Am J Med Genet; 1999 Mar; 83(2):109-16. PubMed ID: 10190481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A particular form of cranio-facio-mandibular dysostosis with type B brachydactylia.
    Van Damme W; Touitou D
    J Belge Radiol; 1980; 63(4):491-6. PubMed ID: 7204325
    [No Abstract]   [Full Text] [Related]  

  • 6. [Hypertelorism].
    de Hauwere R; Vanheule R
    J Belge Radiol; 1972; 55(6):607-8. PubMed ID: 4661488
    [No Abstract]   [Full Text] [Related]  

  • 7. A case of Freeman-Sheldon syndrome (cranio-carpotarsal dysplasia) with spatulate ("canoe paddle") ribs.
    Patel M; Mahmud F
    Br J Radiol; 1983 Jan; 56(661):50-1. PubMed ID: 6821743
    [No Abstract]   [Full Text] [Related]  

  • 8. The W syndrome. Studies of malformation syndromes of man XXVIII.
    Pallister PD; Herrmann J; Spranger JW; Gorlin RJ; Langer LO; Opitz JM
    Birth Defects Orig Artic Ser; 1974; 10(7):51-60. PubMed ID: 4425540
    [No Abstract]   [Full Text] [Related]  

  • 9. [Clinical variations in Léri-Weill dyschondrosteosis].
    Duro EA; Prado GS
    An Esp Pediatr; 1990 Nov; 33(5):461-3. PubMed ID: 2096761
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Neonatal death dwarfism.
    Kozlowski K; Masel J; Morris L; Ryan J; Collins E; Van Vliet P; Woolnough H
    Australas Radiol; 1977 Jun; 21(2):164-83. PubMed ID: 566541
    [No Abstract]   [Full Text] [Related]  

  • 11. [Radiologic diagnosis of Nager syndrome].
    Dammert S; Funke M; Merten HA
    Rofo; 2001 Dec; 173(12):1147-8. PubMed ID: 11740677
    [No Abstract]   [Full Text] [Related]  

  • 12. A sporadic case of apparent Crouzon's syndrome with extracraniofacial manifestations.
    Leonard MA
    J Med Genet; 1974 Jun; 11(2):206-8. PubMed ID: 4367193
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Stomatological features of cranio-facial dysostosis].
    Rusu M; Scintei V; Socolovschi M; Harmanschi A
    Rev Stomatol Chir Maxillofac; 1972 Mar; 73(2):123-31. PubMed ID: 4506595
    [No Abstract]   [Full Text] [Related]  

  • 14. The VSR syndrome. Studies of malformation syndromes of man XXXII.
    Herrmann J; Opitz JM
    Birth Defects Orig Artic Ser; 1974; 10(9):227-39. PubMed ID: 4425539
    [No Abstract]   [Full Text] [Related]  

  • 15. [Hypertelorism and other congenital malformations in a family].
    Freund MM
    J Genet Hum; 1973 Dec; 21(4):237-78. PubMed ID: 4792237
    [No Abstract]   [Full Text] [Related]  

  • 16. Craniofacial dysostosis (Crouzon's disease) associated with metaphyseal dysplasia (Pyle's disease) in the same subject. A roentgenologic study.
    Nardi P; Biagi P; Poggini M; Mara M
    Panminerva Med; 1989; 31(4):192-7. PubMed ID: 2633110
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Familial acromelic frontonasal dysostosis: autosomal dominant inheritance with reduced penetrance.
    Hing AV; Syed N; Cunningham ML
    Am J Med Genet A; 2004 Aug; 128A(4):374-82. PubMed ID: 15264282
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The genetics of hand malformations.
    Temtamy SA; McKusick VA
    Birth Defects Orig Artic Ser; 1978; 14(3):i-xviii, 1-619. PubMed ID: 215242
    [No Abstract]   [Full Text] [Related]  

  • 19. Pycnodysostosis.
    Suma TK; Roy VC
    J Assoc Physicians India; 1986 Nov; 34(11):811-3. PubMed ID: 3558310
    [No Abstract]   [Full Text] [Related]  

  • 20. Syndrome of a craniofacial dysostosis, limb malformation, and omphalocele.
    Gardner RJ; Morrison PS; Faigan LA; Kennedy JC; Fitzgerald PH
    Am J Med Genet; 1990 Jun; 36(2):133-6. PubMed ID: 2368799
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.