BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

195 related articles for article (PubMed ID: 7361736)

  • 1. Campomelic dysplasia. Further elucidation of a distinct entity.
    Hall BD; Spranger JW
    Am J Dis Child; 1980 Mar; 134(3):285-9. PubMed ID: 7361736
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Campomelic dysplasia: evidence of autosomal dominant inheritance.
    Lynch SA; Gaunt ML; Minford AM
    J Med Genet; 1993 Aug; 30(8):683-6. PubMed ID: 8411055
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genetics of short stature.
    Scott CI
    Prog Med Genet; 1972; 8():243-99. PubMed ID: 4259833
    [No Abstract]   [Full Text] [Related]  

  • 4. [Camptomelic dysplasia. A case of survival for more than 4 years].
    Noyal P; Vermeulin G; Hibon D; Meck JM
    Arch Fr Pediatr; 1982 Oct; 39(8):621-4. PubMed ID: 7159163
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Congenital familial dwarfism with cephalo-skeletal dysplasia.
    Thomas PS; Nevin NC
    Ann Radiol (Paris); 1976; 19(1):187-92. PubMed ID: 984702
    [No Abstract]   [Full Text] [Related]  

  • 6. [A case of chondrodysplasia difficult to classify: metatropic dwarfism or Kozlowski type spondylometaphyseal dysplasia?].
    Vallcanera A; Lanuza A; Cortina H; Aparici R
    Ann Radiol (Paris); 1977 Jun; 20(5):527-30. PubMed ID: 900812
    [No Abstract]   [Full Text] [Related]  

  • 7. Heterogeneity in the campomelic syndromes. Long-and short-bone varieties.
    Khajavi A; Lachman R; Rimoin D; Schimke RN; Dorst J; Handmaker S; Ebbin A; Perreault G
    Radiology; 1976 Sep; 120(3):641-7. PubMed ID: 948600
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A probably distinct autosomal recessive thoraco-limb dysplasia.
    Rivera H; Perez-Salas JM; Nazara Z; Ramirez ML
    J Med Genet; 1988 Sep; 25(9):619-22. PubMed ID: 3184141
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The SPONASTRIME dysplasia: familial short-limb dwarfism with saddle nose, spinal alterations and metaphyseal striation. Report of 4 siblings.
    Fanconi S; Issler C; Giedion A; Prader A
    Helv Paediatr Acta; 1983 Aug; 38(3):267-80. PubMed ID: 6618893
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Short rib-polydactyly syndrome, Majewski type.
    Chen H; Yang SS; Gonzalez E; Fowler M; Al Saadi A
    Am J Med Genet; 1980; 7(2):215-22. PubMed ID: 7468649
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A possibly new form of familial bone dysplasia resembling dyschondrosteosis.
    Fasanelli S; Iannaccone G; Bellussi A
    Pediatr Radiol; 1983; 13(1):25-31. PubMed ID: 6844051
    [No Abstract]   [Full Text] [Related]  

  • 13. An autosomal recessive form of lethal chondrodystrophy with severe thoracic narrowing, rhizoacromelic type of micromelia, polydacytly and genital anomalies.
    Verma IC; Bhargava S; Agarwal S
    Birth Defects Orig Artic Ser; 1975; 11(6):167-74. PubMed ID: 1103993
    [No Abstract]   [Full Text] [Related]  

  • 14. [Campomelic dwarfism. Its placement in the heterogeneous group of congenital bowing of the limbs].
    Nardini C; Sordato S
    Pediatr Med Chir; 1985; 7(2):259-70. PubMed ID: 4094914
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dwarfism in the newborn: the nomenclature, radiological features and genetic significance.
    Cremin BJ; Beighton P
    Br J Radiol; 1974 Feb; 47(554):77-93. PubMed ID: 4206212
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. 3-Year-old phenotypic female with campomelic dysplasia and bilateral gonadoblastoma.
    Hong JR; Barber M; Scott CI; Guttenberg M; Wolfson PJ
    J Pediatr Surg; 1995 Dec; 30(12):1735-7. PubMed ID: 8749940
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial rhizomelic dysplasia: phenotypic variation or heterogeneity?
    Viljoen D; Goldblatt J; Wallis C; Beighton P
    Am J Med Genet; 1987 Apr; 26(4):941-7. PubMed ID: 3591839
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Congenital familial dwarfism with cephaloskeletal dysplasia (Taybi-Linder syndrome)].
    Lavollay B; Faure C; Filipe G; Branca G; Huet de Barochez Y
    Arch Fr Pediatr; 1984 Jan; 41(1):57-60. PubMed ID: 6721654
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neonatal lethal dwarfism with distinct skeletal malformations--a separate entity?
    Rosendahl K; Maurseth K; Olsen ØE ; Halvorsen OJ; Gjelland K; Engebretsen L
    Pediatr Radiol; 2001 Sep; 31(9):663-8. PubMed ID: 11512011
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.