BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 9450878)

  • 1. Dyssegmental dysplasia Silverman-Handmaker type in a consanguineous Druze Lebanese family: long term survival and documentation of the natural history.
    Prabhu VG; Kozma C; Leftridge CA; Helmbrecht GD; France ML
    Am J Med Genet; 1998 Jan; 75(2):164-70. PubMed ID: 9450878
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Evidence of heterogeneity in dyssegmental dysplasia].
    Oliván Gonzalvo G; Bueno Sánchez M
    An Esp Pediatr; 1990 Sep; 33(3):213-23. PubMed ID: 2285185
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dyssegemental dyspalsia; Rolland-Desbuquois type--a case report from Pakistan.
    Afroze B
    J Pak Med Assoc; 2010 Apr; 60(4):312-3. PubMed ID: 20419979
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Dyssegmental dysplasia, Silverman-Handmaker type: A challenging antenatal diagnosis in a dizygotic twin pregnancy.
    Basalom S; Trakadis Y; Shear R; Azouz ME; De Bie I
    Mol Genet Genomic Med; 2018 May; 6(3):452-456. PubMed ID: 29526034
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Dyssegmental dysplasia: a case report of a Rolland-Desbuquois type.
    d'Orey MC; Mateus M; Guimarães H; Miguel C; Costeira MJ; Nogueira R; Montenegro N; Santos NT; Maroteaux P
    Pediatr Radiol; 1997 Dec; 27(12):948-50. PubMed ID: 9388290
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dyssegmental dysplasia with glaucoma.
    Maroteaux P; Manouvrier S; Bonaventure J; Le Merrer M
    Am J Med Genet; 1996 May; 63(1):46-9. PubMed ID: 8723085
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotypic and molecular characterization of a novel case of dyssegmental dysplasia, Silverman-Handmaker type.
    Rieubland C; Jacquemont S; Mittaz L; Osterheld MC; Vial Y; Superti-Furga A; Unger S; Bonafé L
    Eur J Med Genet; 2010; 53(5):294-8. PubMed ID: 20542149
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Dyssegmental dysplasias: clinical, radiographic, and morphologic evidence of heterogeneity.
    Aleck KA; Grix A; Clericuzio C; Kaplan P; Adomian GE; Lachman R; Rimoin DL
    Am J Med Genet; 1987 Jun; 27(2):295-312. PubMed ID: 3605216
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literature.
    Sigaudy S; Toutain A; Moncla A; Fredouille C; Bourlière B; Ayme S; Philip N
    Am J Med Genet; 1998 Oct; 80(1):16-24. PubMed ID: 9800907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dyssegmental dysplasia, Silverman-Handmaker type, is caused by functional null mutations of the perlecan gene.
    Arikawa-Hirasawa E; Wilcox WR; Le AH; Silverman N; Govindraj P; Hassell JR; Yamada Y
    Nat Genet; 2001 Apr; 27(4):431-4. PubMed ID: 11279527
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prevalence of lethal osteochondrodysplasias in Denmark.
    Andersen PE
    Am J Med Genet; 1989 Apr; 32(4):484-9. PubMed ID: 2789000
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Dyssegmental dwarfism--report on two cases (author's transl)].
    Miething R; Stöver B; Tuengerthal S; Winterling D; Svejcar J
    Radiologe; 1981 Apr; 21(4):190-4. PubMed ID: 7220870
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The Dyggve-Melchior-Clausen syndrome in adult siblings.
    Bonafede RP; Beighton P
    Clin Genet; 1978 Jul; 14(1):24-30. PubMed ID: 679519
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sporadic case of dyssegmental dysplasia with antenatal presentation.
    Stoll C; Langer B; Gasser B; Alembik Y
    Genet Couns; 1998; 9(2):125-30. PubMed ID: 9664209
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Dwarfism, dyssegmental, Silverman-Handmaker type].
    Sonoda T
    Ryoikibetsu Shokogun Shirizu; 2001; (33):578-9. PubMed ID: 11462578
    [No Abstract]   [Full Text] [Related]  

  • 17. Dyssegmental dysplasia in siblings: prenatal ultrasonic diagnosis.
    Andersen PE; Hauge M; Bang J
    Skeletal Radiol; 1988; 17(1):29-31. PubMed ID: 3282308
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2.
    Cormier-Daire V; Superti-Furga A; Munnich A; Lyonnet S; Rustin P; Delezoide AL; De Lonlay P; Giedion A; Maroteaux P; Le Merrer M
    Am J Med Genet; 1998 Jun; 78(2):146-9. PubMed ID: 9674905
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.