BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 5713631)

  • 1. Three recessive mutations producing disproportionate dwarfing in mice: achondroplasia, brachymorphic, and stubby.
    Lane PW; Dickie MM
    J Hered; 1968; 59(5):300-8. PubMed ID: 5713631
    [No Abstract]   [Full Text] [Related]  

  • 2. A new type of chondrodystrophic mutant in the mouse.
    Ferguson JM; Wallace ME; Johnson DR
    J Med Genet; 1978 Apr; 15(2):128-31. PubMed ID: 641946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defective endochondral ossification in brachymorphic mice.
    Silberberg R; Lesker P
    J Comp Pathol; 1977 Apr; 87(2):319-23. PubMed ID: 858816
    [No Abstract]   [Full Text] [Related]  

  • 4. Short-limbed dwarfism and ocular defects in the Samoyed dog.
    Meyers VN; Jezyk PF; Aguirre GD; Patterson DF
    J Am Vet Med Assoc; 1983 Nov; 183(9):975-9. PubMed ID: 12002589
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Dwarfism in red Danish cattle (bovine achondroplasia: type RDM) (author's transl)].
    Andresen E; Christensen K; Jensen PT; Venge O; Rasmussen PG; Basse A; Neimann-Sorensen A; Jensen B; Nielsen J
    Nord Vet Med; 1974 Dec; 26(12):681-91. PubMed ID: 4449723
    [No Abstract]   [Full Text] [Related]  

  • 6. [Clinical analysis and genetic diagnosis of short-limb inherited short stature diseases in children].
    Li F; Ma HW; Song Y; Hu M; Ren S; Yu YF; Zhao GJ
    Zhongguo Dang Dai Er Ke Za Zhi; 2013 Nov; 15(11):932-6. PubMed ID: 24229583
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel hypothyroid dwarfism due to the missense mutation Arg479Cys of the thyroid peroxidase gene in the mouse.
    Takabayashi S; Umeki K; Yamamoto E; Suzuki T; Okayama A; Katoh H
    Mol Endocrinol; 2006 Oct; 20(10):2584-90. PubMed ID: 16762971
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A chondroplastic, brachymorphic and stubby chondrodystophies in mice.
    Miller WA; Flynn-Miller KL
    J Comp Pathol; 1976 Jul; 86(3):349-63. PubMed ID: 939824
    [No Abstract]   [Full Text] [Related]  

  • 9. Low bone mineral density in achondroplasia and hypochondroplasia.
    Matsushita M; Kitoh H; Mishima K; Kadono I; Sugiura H; Hasegawa S; Nishida Y; Ishiguro N
    Pediatr Int; 2016 Aug; 58(8):705-8. PubMed ID: 26716907
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cataract--webbed Peromyscus. I. Genetics of cataract in P. maniculatus.
    Anderson RS; Burns RP
    J Hered; 1979; 70(1):27-30. PubMed ID: 469220
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Children with short-limbed short stature in pediatric endocrinological services in Japan.
    Hasegawa K; Tanaka H
    Pediatr Int; 2014 Dec; 56(6):809-812. PubMed ID: 25244068
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A single nucleotide mutation in Nppc is associated with a long bone abnormality in lbab mice.
    Jiao Y; Yan J; Jiao F; Yang H; Donahue LR; Li X; Roe BA; Stuart J; Gu W
    BMC Genet; 2007 Apr; 8():16. PubMed ID: 17439653
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [HYPOCHONDROPLASIA].
    KOZLOWSKI K; ZYCHOWICZ C
    Fortschr Geb Rontgenstr Nuklearmed; 1964 Apr; 100():529-35. PubMed ID: 14199851
    [No Abstract]   [Full Text] [Related]  

  • 14. Chubby: a new autosomal recessive skeletal mutation producing dwarfism in the mouse.
    Wikström B; Wallace ME; Hjerpe A; Engfeldt B
    J Hered; 1987; 78(1):8-14. PubMed ID: 3571949
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [HYPOCHONDROPLASIA (A FURTHER CONTRIBUTION)].
    KOZLOWSKI K; ZYCHOWICZ C
    Fortschr Geb Rontgenstr Nuklearmed; 1964 Nov; 101():531-5. PubMed ID: 14337160
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetics of the Alaskan Malmute chondrodysplasia syndrome.
    Subden RE; Fletch SM; Smart MA; Brown RG
    J Hered; 1972; 63(3):149-52. PubMed ID: 4537780
    [No Abstract]   [Full Text] [Related]  

  • 17. C-type natriuretic peptide plasma levels are elevated in subjects with achondroplasia, hypochondroplasia, and thanatophoric dysplasia.
    Olney RC; Prickett TC; Espiner EA; Mackenzie WG; Duker AL; Ditro C; Zabel B; Hasegawa T; Kitoh H; Aylsworth AS; Bober MB
    J Clin Endocrinol Metab; 2015 Feb; 100(2):E355-9. PubMed ID: 25387261
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myodystrophy, a new myopathy on chromosome 8 of the mouse.
    Lane PW; Beamer TC; Myers DD
    J Hered; 1976; 67(3):135-8. PubMed ID: 939913
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotype-based search of natural mutations related to hereditary diseases existing in a closed colony of mice.
    Katoh H; Nishikawa T; Kimura J; Yamauchi Y; Takabayashi S
    Exp Anim; 2010; 59(2):183-90. PubMed ID: 20484851
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Evidence for allelism of leaner and tottering in the mouse.
    Tsuji S; Meier H
    Genet Res; 1971 Feb; 17(1):83-8. PubMed ID: 4933322
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.