BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 9716634)

  • 1. 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]  

  • 2. Autosomal recessive omodysplasia.
    Stoll C; Pennerath A; Poirat P
    Ann Genet; 1995; 38(2):97-101. PubMed ID: 7486832
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recessive omodysplasia: five new cases and review of the literature.
    Elçioglu NH; Gustavson KH; Wilkie AO; Yüksel-Apak M; Spranger JW
    Pediatr Radiol; 2004 Jan; 34(1):75-82. PubMed ID: 14566439
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Omodysplasia: the first reported Brazilian case.
    Albano LM; Oliveira LA; Bertola DR; Mazzu JF; Kim CA
    Clinics (Sao Paulo); 2007 Aug; 62(4):531-4. PubMed ID: 17823719
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia and distinctive facial appearance.
    al-Gazali LI; Bakalinova D
    Clin Dysmorphol; 1998 Jul; 7(3):177-84. PubMed ID: 9689990
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Spondylo-epiphyseal dysplasia associated with craniosynostosis, cleft palate and mental retardation. A case report].
    Herrera-Martínez AD; Estrada-Corona P
    Invest Clin; 2010 Dec; 51(4):553-60. PubMed ID: 21365879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Long-term observation of a patient with dominant omodysplasia.
    Gordon BL; Champaigne NL; Rogers RC; Frias JL; Leroy JG
    Am J Med Genet A; 2014 May; 164A(5):1234-8. PubMed ID: 24458798
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Familial congenital micromelic dysplasia with dislocation of radius and distinct face: a new skeletal dysplasia syndrome.
    Borochowitz Z; Barak M; Hershkowitz S
    Am J Med Genet; 1991 Apr; 39(1):91-6. PubMed ID: 1867270
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Metaphyseal anadysplasia in two sisters.
    Slama M; Mathieu M; Dehouck I; al Hosri J; Vanthournout I; Baratte B; Grumbach Y
    Pediatr Radiol; 1999 May; 29(5):372-5. PubMed ID: 10382218
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Nonsense mutations in FZD2 cause autosomal-dominant omodysplasia: Robinow syndrome-like phenotypes.
    Nagasaki K; Nishimura G; Kikuchi T; Nyuzuki H; Sasaki S; Ogawa Y; Saitoh A
    Am J Med Genet A; 2018 Mar; 176(3):739-742. PubMed ID: 29383834
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Omodysplasia.
    Maroteaux P; Sauvegrain J; Chrispin A; Farriaux JP
    Am J Med Genet; 1989 Mar; 32(3):371-5. PubMed ID: 2729357
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic features.
    Langer LO; Wolfson BJ; Scott CI; Reid CS; Schidlow DV; Millar EA; Borns PF; Lubicky JP; Carpenter BL
    Am J Med Genet; 1993 Feb; 45(4):488-500. PubMed ID: 8465857
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Autosomal recessive spondylometaphyseal dysplasia. Apropos of 3 familial cases].
    Meziane AO; Meziane A; Ksiyer M; Bennani-Smires C; Khalifa HH
    Ann Genet; 1987; 30(4):216-20. PubMed ID: 3501265
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Holoprosencephaly and primary craniosynostosis: the Genoa syndrome.
    Camera G; Lituania M; Cohen MM
    Am J Med Genet; 1993 Dec; 47(8):1161-5. PubMed ID: 8291548
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.