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Journal Abstract Search

288 related items for PubMed ID: 2306591

  • 1. The radiology of Coffin-Lowry syndrome.
    Padley S, Hodgson SV, Sherwood T.
    Br J Radiol; 1990 Jan; 63(745):72-5. PubMed ID: 2306591
    [No Abstract] [Full Text] [Related]

  • 2. Frontometaphyseal dysplasia.
    Holt JF, Thompson GR, Arenberg IK.
    Radiol Clin North Am; 1972 Aug; 10(2):225-43. PubMed ID: 5044403
    [No Abstract] [Full Text] [Related]

  • 3. Roentgenographic manifestations of the Prader-Willi syndrome.
    Pearson KD, Steinbach HL, Bier DM.
    Radiology; 1971 Aug; 100(2):369-77. PubMed ID: 5147402
    [No Abstract] [Full Text] [Related]

  • 4. The Coffin-Lowry syndrome.
    Young ID.
    J Med Genet; 1988 May; 25(5):344-8. PubMed ID: 3290491
    [No Abstract] [Full Text] [Related]

  • 5. The W syndrome. Studies of malformation syndromes of man XXVIII.
    Pallister PD, Herrmann J, Spranger JW, Gorlin RJ, Langer LO, Opitz JM.
    Birth Defects Orig Artic Ser; 1974 May; 10(7):51-60. PubMed ID: 4425540
    [No Abstract] [Full Text] [Related]

  • 6. Syndrome of short stature, microcephaly, mental retardation, and multiple epiphyseal dysplasia--Lowry-Wood syndrome.
    Nevin NC, Thomas PS, Hutchinson J.
    Am J Med Genet; 1986 May; 24(1):33-9. PubMed ID: 3706411
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  • 9. [Rubinstein-Taybi-Syndrome in premature, probably identical twins].
    Holthusen W, Panteliadis C.
    Monatsschr Kinderheilkd (1902); 1971 Sep; 119(9):523-7. PubMed ID: 5097246
    [No Abstract] [Full Text] [Related]

  • 10. Radiographic findings in Shprintzen-Goldberg syndrome.
    Nishimura G, Nagai T.
    Pediatr Radiol; 1996 Nov; 26(11):775-8. PubMed ID: 8929375
    [Abstract] [Full Text] [Related]

  • 11. A Croatian case of the Schinzel-Giedion syndrome.
    Culić V, Resic B, Oorthuys JW, Overweg-Plandsoen WC, Hennekam RC.
    Genet Couns; 1996 Nov; 7(1):21-5. PubMed ID: 8652084
    [Abstract] [Full Text] [Related]

  • 12. Deletion of 16q with prolonged survival and unusual radiographic manifestations.
    Casamassima AC, Klein RM, Wilmot PL, Brenholz P, Shapiro LR.
    Am J Med Genet; 1990 Dec; 37(4):504-9. PubMed ID: 2260595
    [Abstract] [Full Text] [Related]

  • 13. Coffin-Lowry syndrome: a multicenter study.
    Gilgenkrantz S, Mujica P, Gruet P, Tridon P, Schweitzer F, Nivelon-Chevallier A, Nivelon JL, Couillault G, David A, Verloes A.
    Clin Genet; 1988 Oct; 34(4):230-45. PubMed ID: 3069251
    [Abstract] [Full Text] [Related]

  • 14. Brief clinical report: early recognition of the Coffin-Lowry syndrome.
    Wilson WG, Kelly TE.
    Am J Med Genet; 1981 Oct; 8(2):215-20. PubMed ID: 7282775
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  • 18. [Cloverleaf skull associated with generalized bone defects close to asphyxiating thoracic dysplasia].
    Benallègue A, Lacete F, Maroteaux P.
    Ann Genet; 1987 Oct; 30(2):113-7. PubMed ID: 3499843
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  • 19. Megadolichosigmoid in a young male with Aarskog syndrome.
    Casteels M, Samain H, Penninckx F, Coremans G, Beirinckx J, Fryns JP.
    Genet Couns; 1994 Oct; 5(1):81-3. PubMed ID: 8031541
    [No Abstract] [Full Text] [Related]

  • 20. [Association of Saethre-Chotzen and fra-X syndrome].
    Fehlow P, Miosge W, Walther F.
    Klin Padiatr; 1994 Oct; 206(5):410-1. PubMed ID: 7799621
    [Abstract] [Full Text] [Related]

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