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Journal Abstract Search

263 related items for PubMed ID: 819054

  • 1. Malformation syndromes. A selected miscellany.
    Gorlin RJ, Cervenka J, Moller K, Horrobin M, Witkop CJ.
    Birth Defects Orig Artic Ser; 1975; 11(2):39-50. PubMed ID: 819054
    [No Abstract] [Full Text] [Related]

  • 2. [The Coffin-Siris syndrome. A new syndrome of mental retardation, hypo-aplasia of the nails and terminal phalanges of the 5th fingers and toes].
    Mastroiacovo P, Salvaggio E, Parenti D.
    Minerva Pediatr; 1977 Mar 31; 29(11):773-8. PubMed ID: 875947
    [No Abstract] [Full Text] [Related]

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  • 4. [Ullrich-Feichtiger syndrome in a 3-year-old boy].
    Mazur B, Buszman Z.
    Pol Tyg Lek; 1977 Mar 31; 47(9-10):234-5. PubMed ID: 1437827
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  • 5. [The Coffin-Siris syndrome. Case report].
    Giovannucci Uzielli ML, Seminara S, Nicòtina PA, Consumi I, La Cauza C.
    Minerva Pediatr; 1980 Feb 28; 32(4):245-54. PubMed ID: 6770244
    [No Abstract] [Full Text] [Related]

  • 6. Trisomy 8: an international study of 70 patients.
    Riccardi VM.
    Birth Defects Orig Artic Ser; 1977 Feb 28; 13(3C):171-84. PubMed ID: 890109
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  • 7. The extra digit. A pointer to the eye?
    Calver D, Keast-Butler J, Taylor D.
    Trans Ophthalmol Soc U K (1962); 1981 Feb 28; 101(1):35-8. PubMed ID: 6821009
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  • 10. [A rare dysplasia: the oculo-dento-digital syndrome].
    Sörgel HJ, Heidrich R.
    Z Arztl Fortbild (Jena); 1965 May 01; 59(9):504-6. PubMed ID: 4957703
    [No Abstract] [Full Text] [Related]

  • 11. [Coffin-Siris syndrome in a 5-year-old girl].
    Meinecke P, Engelbrecht R, Schaefer E.
    Monatsschr Kinderheilkd; 1986 Sep 01; 134(9):692-5. PubMed ID: 3785238
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  • 12. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E, Stetka DG.
    Am J Med Genet; 1990 May 01; 36(1):11-4. PubMed ID: 2333899
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  • 18. [Weill-Marchesani syndrome].
    Sellem C, Rosenberg D, Chatelain R, Picaud S, Monnet P.
    Pediatrie; 1970 May 01; 25(7):771-5. PubMed ID: 4991254
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  • 19. Mosaic trisomy 9 syndrome with unusual phenotype.
    Kaminker CP, Daín L, Lamas MA, Sánchez JM.
    Am J Med Genet; 1985 Oct 01; 22(2):237-41. PubMed ID: 3931476
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  • 20. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Oct 01; 8(4):839-910. PubMed ID: 4244691
    [No Abstract] [Full Text] [Related]

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