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Journal Abstract Search

174 related items for PubMed ID: 6954841

  • 1. [Description of an orofaciodigital syndrome].
    Joosen E, Legrand W.
    Acta Stomatol Belg; 1982; 79(1):45-54. PubMed ID: 6954841
    [No Abstract] [Full Text] [Related]

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  • 4. [Case of Arskog is syndrome].
    Chen TP, Romanenko OP, Shats VIa, Sandomirskaia LM, Azarova VIa.
    Pediatriia; 1980 Apr; (4):60-1. PubMed ID: 7189853
    [No Abstract] [Full Text] [Related]

  • 5. [The Mohr syndrome (orofaciodigital syndrome type II). 1 familial case].
    Cotton JB, Gardet R, Ladreyt JP, Guibaud P.
    Pediatrie; 1979 Apr; 34(3):257-66. PubMed ID: 492868
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  • 7. Orofaciodigital syndrome type IV: report of a patient.
    Nevin NC, Thomas PS.
    Am J Med Genet; 1989 Feb; 32(2):151-4. PubMed ID: 2929654
    [Abstract] [Full Text] [Related]

  • 8. Orofaciodigital syndrome II (OFD II) in brother and sister.
    Jorgenson RJ.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):271-2. PubMed ID: 5173223
    [No Abstract] [Full Text] [Related]

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  • 11. Letter: Orofaciodigital syndrome.
    Melnick M, Shields ED.
    Clin Genet; 1976 Jul; 10(1):61. PubMed ID: 949866
    [No Abstract] [Full Text] [Related]

  • 12. Coffin-Lowry syndrome in an Afro-American family.
    Kousseff BG.
    Am J Med Genet; 1982 Mar; 11(3):373-5. PubMed ID: 7081302
    [No Abstract] [Full Text] [Related]

  • 13. Oral-facial-skeletal syndromes.
    Neri G, Gurrieri F, Genuardi M.
    Am J Med Genet; 1995 Nov 20; 59(3):365-8. PubMed ID: 8599363
    [No Abstract] [Full Text] [Related]

  • 14. [Freeman-Sheldon syndrome. Description of 2 cases of probable recessive autosomal inheritance].
    Bonioli E, Bellini C, Ruffa G, Lagorio V, Gemme G.
    Minerva Pediatr; 1987 Feb 28; 39(3-4):123-7. PubMed ID: 3587189
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  • 15. [Orofaciodigital syndrome type I in a mother and daughter].
    Guerrero Vázquez J, Cazenave Bernal A, de Paz Aparicio P, Luengo Casasola JL, Garcés Ramos A, López Vázquez JL, Hoyos Madrid JJ.
    An Esp Pediatr; 1988 Jan 28; 28(1):59-62. PubMed ID: 3279888
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  • 16. [Aarskog's syndrome. Description of a familial case].
    Tucciarone L, De Santis F, Ballati G, Latini M, Felici W.
    Minerva Pediatr; 1987 Apr 30; 39(8):341-6. PubMed ID: 3614163
    [No Abstract] [Full Text] [Related]

  • 17. A contribution to the genetics of oral-facial-digital (OFD) syndrome.
    Chaurasia BD, Goswami HK.
    Jinrui Idengaku Zasshi; 1973 Dec 30; 18(3):294-9. PubMed ID: 4800018
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  • 18. [Orofaciodigital syndrome].
    Hille M, Pelz L, Andrä A, Tolksdorff B, Dittmer J.
    Kinderarztl Prax; 1971 Feb 30; 39(2):68-76. PubMed ID: 5088971
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  • 19. Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1.
    Cohen MM, Charrow J, Nadler HL.
    Am J Hum Genet; 1981 Jul 30; 33(4):649-50. PubMed ID: 7258190
    [No Abstract] [Full Text] [Related]

  • 20. Metaphyseal dysplasia with maxillary hypoplasia and brachydactyly.
    Halal F, Picard JL, Raymond-Tremblay D, de Bosset P.
    Am J Med Genet; 1982 Sep 30; 13(1):71-9. PubMed ID: 7137223
    [Abstract] [Full Text] [Related]

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