BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 1416547)

  • 1. [Campomelic dysplasia: apropos of a case].
    González-Ripoll Garzón M; Durán Román M; Cañabate Reche F; Martín González M; López Muñoz J
    An Esp Pediatr; 1992 Aug; 37(2):166-8. PubMed ID: 1416547
    [No Abstract]   [Full Text] [Related]  

  • 2. Acampomelic campomelic dysplasia.
    Macpherson RI; Skinner SA; Donnenfeld AE
    Pediatr Radiol; 1989; 20(1-2):90-3. PubMed ID: 2602025
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Presentation of six cases of Stüve-Wiedemann syndrome.
    Cormier-Daire V; Munnich A; Lyonnet S; Rustin P; Delezoide AL; Maroteaux P; Le Merrer M
    Pediatr Radiol; 1998 Oct; 28(10):776-80. PubMed ID: 9799300
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Infant with manifestations of oto-palato-digital syndrome type II and of Melnick-Needles syndrome.
    Corona-Rivera JR; Corona-Rivera E; Corona-Rivera A; Quiles-Corona M; Velez-Gómez E; Arana-Gutiérrez MA
    Am J Med Genet; 1999 Jul; 85(1):79-81. PubMed ID: 10377016
    [No Abstract]   [Full Text] [Related]  

  • 5. [Camptomelic dysplasia. Apropos of a case].
    Gnamey DK; Eynard JP
    Pediatrie; 1984 Sep; 39(6):455-9. PubMed ID: 6527921
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pathological case of the month. Campomelic dysplasia.
    Iravani S; Debich-Spicer D; Gilbert-Barness E
    Arch Pediatr Adolesc Med; 2000 Jul; 154(7):747-8. PubMed ID: 10891031
    [No Abstract]   [Full Text] [Related]  

  • 7. Fibrochondrogenesis: clinical and radiological features.
    al-Gazali LI; Bakalinova D; Bakir M; Dawodu A
    Clin Dysmorphol; 1997 Apr; 6(2):157-63. PubMed ID: 9134297
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CODAS syndrome: a new distinct MCA/MR syndrome with radiological changes of spondyloepiphyseal dysplasia. Another case report.
    de Almeida JC; Vargas FR; Barbosa-Neto JG; Llerena JC
    Am J Med Genet; 1995 Jan; 55(1):19-20. PubMed ID: 7702089
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Fatal genetic-morphologic syndromes. The campomelic syndrome].
    Henkel KE; Pfeiffer RA; Stöss H
    Pathologe; 1993 May; 14(3):162-4. PubMed ID: 8516273
    [No Abstract]   [Full Text] [Related]  

  • 10. Spondyloepimetaphyseal dysplasia with joint laxity (SEMDJL) in three neonates.
    Christianson AL; Beighton P
    Genet Couns; 1996; 7(3):219-25. PubMed ID: 8897044
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Omodysplasia: an affected mother and son.
    Venditti CP; Farmer J; Russell KL; Friedrich CA; Alter C; Canning D; Whitaker L; Mennuti MT; Driscoll DA; Zackai EH
    Am J Med Genet; 2002 Aug; 111(2):169-77. PubMed ID: 12210345
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Previously unrecognized form of familial spondyloepiphyseal dysplasia tarda with characteristic facies.
    Huson SM; Crowley S; Hall CM; Supramaniam G; Winter RM
    Clin Dysmorphol; 1993 Jan; 2(1):20-7. PubMed ID: 8298734
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diastrophic dysplasia: extreme variability within a sibship.
    Hall BD
    Am J Med Genet; 1996 May; 63(1):28-33. PubMed ID: 8723083
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Description of a case of thanatophoric dysplasia with cloverleaf skull].
    Ronconi GF; Pesenti P; Mercurella A; Sassolino S
    Pediatr Med Chir; 1986; 8(3):423-5. PubMed ID: 3786207
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Recent progress in biochemical and histological research during Morquio's disease. Report of three new cases].
    Attal P
    Ann Pediatr (Paris); 1977 Feb; 24(2):153-9. PubMed ID: 16211956
    [No Abstract]   [Full Text] [Related]  

  • 16. Abnormal oral-pharyngeal swallowing as cause of morbidity and early death in Stüve-Wiedemann syndrome.
    Corona-Rivera JR; Cormier-Daire V; Dagoneau N; Coello-Ramírez P; López-Marure E; Romo-Huerta CO; Silva-Baez H; Aguirre-Salas LM; Estrada-Solorio MI
    Eur J Med Genet; 2009; 52(4):242-6. PubMed ID: 19371797
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Lethal osteo-chondro-dysplasia: feto-pathological study of 32 cases].
    Lahmar-Boufaroua A; Yacoubi MT; Hmisssa S; Selmi M; Korbi S
    Tunis Med; 2009 Feb; 87(2):127-32. PubMed ID: 19522446
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autosomal recessive omodysplasia: report of three additional cases.
    Masel JP; Kozlowski K; Kiss P
    Pediatr Radiol; 1998 Aug; 28(8):608-11. PubMed ID: 9716634
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation.
    Young ID; Zuccollo JM; Maltby EL; Broderick NJ
    J Med Genet; 1992 Apr; 29(4):251-2. PubMed ID: 1583645
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 11.