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Journal Abstract Search

280 related items for PubMed ID: 6710469

  • 21. [Chondrodysplasia punctata (author's transl)].
    Boroń Z, Balcar-Boroń A, Słowik J.
    Monatsschr Kinderheilkd (1902); 1980 Feb; 128(2):104-5. PubMed ID: 7360129
    [Abstract] [Full Text] [Related]

  • 22. [Some aspects of chondrodystrophia calcificans congenita].
    Bergström K, Gustavson KH, Jorulf H.
    Nord Med; 1971 May 20; 85(20):634. PubMed ID: 5580911
    [No Abstract] [Full Text] [Related]

  • 23. Chondrodysplasia punctata. Conradi-Hünermann syndrome.
    Edidin DV, Esterly NB, Bamzai AK, Fretzin DF.
    Arch Dermatol; 1977 Oct 20; 113(10):1431-4. PubMed ID: 911172
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  • 24. Chondrodysplasia punctata after warfarin. Case report with 18-month follow-up.
    Tamburrini O, Bartolomeo-De Iuri A, Di Guglielmo GL.
    Pediatr Radiol; 1987 Oct 20; 17(4):323-4. PubMed ID: 3601467
    [Abstract] [Full Text] [Related]

  • 25. [Chondroplasia punctata (author's transl)].
    Koischwitz D, Anders G.
    Rofo; 1980 Jun 20; 132(6):689-94. PubMed ID: 6450133
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  • 26. [Chondrodystrophia calcificans congenita in a new genetic light].
    Bergström K, Jorulf H, Thor L, Gustavson KH, Melander S.
    Lakartidningen; 1971 Jun 23; 68(26):3023-6. PubMed ID: 5561853
    [No Abstract] [Full Text] [Related]

  • 27. [Stippled epiphyseal disease in a newborn infant].
    Caron-Poitreau C, Rouchy R, Leroux-Clenet N, Caron J.
    J Radiol Electrol Med Nucl; 1970 May 23; 51(5):296-8. PubMed ID: 5502372
    [No Abstract] [Full Text] [Related]

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  • 31. Peroxisomal dysfunction in chondrodysplasia punctata, rhizomelic type.
    Oorthuys JW, Loewer-Sieger DH, Schutgens RB, Wanders RJ, Heymans HS, Bleeker-Wagemakers EM.
    Ophthalmic Paediatr Genet; 1987 Nov 23; 8(3):183-5. PubMed ID: 3438058
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  • 35. [Chondrodysplasia punctata].
    Jancovic D, Drimal J, Hromec I, Jakubec I.
    Acta Chir Orthop Traumatol Cech; 1990 Jun 23; 57(3):256-64. PubMed ID: 2220236
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  • 37. Brachytelephalangic chondrodysplasia punctata: a possible X-linked recessive form.
    Maroteaux P.
    Hum Genet; 1989 May 23; 82(2):167-70. PubMed ID: 2722194
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