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PUBMED FOR HANDHELDS

Journal Abstract Search

125 related items for PubMed ID: 7189853

  • 1. [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]

  • 2. [A new genetic variant of the orofaciodigital syndrome].
    Bochkova DN, Ternova TI.
    Pediatriia; 1990 Apr; (3):95-6. PubMed ID: 2385482
    [No Abstract] [Full Text] [Related]

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  • 4. The genetics of hand malformations.
    Temtamy SA, McKusick VA.
    Birth Defects Orig Artic Ser; 1978 Apr; 14(3):i-xviii, 1-619. PubMed ID: 215242
    [No Abstract] [Full Text] [Related]

  • 5. X-linked recessive inheritance of an orofaciodigital syndrome with partial expression in females and survival of affected males.
    Edwards M, Mulcahy D, Turner G.
    Clin Genet; 1988 Nov; 34(5):325-32. PubMed ID: 3229001
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  • 7. Coffin-Lowry syndrome in an Afro-American family.
    Kousseff BG.
    Am J Med Genet; 1982 Mar; 11(3):373-5. PubMed ID: 7081302
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  • 10. [Coffin-Lowry syndrome. Description of 2 cases].
    Barajas LO, Rivera H, Fragoso R, Nazara Z, Cantú JM.
    Bol Med Hosp Infant Mex; 1986 Jun; 43(6):378-81. PubMed ID: 3730116
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  • 11. [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(1):59-62. PubMed ID: 3279888
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  • 15. 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
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  • 17. The 47,XXY karyotype and unrelated malformative patterns: an unusual association.
    Aricò M, Colombo A, Maserati E, Pasquali F, Burgio GR.
    Helv Paediatr Acta; 1987 Jun; 42(5-6):457-61. PubMed ID: 3454351
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  • 19. See-saw winking in a familial oral-facial-digital syndrome.
    Sugarman GI, Katakia M, Menkes J.
    Clin Genet; 1971 Jun; 2(4):248-54. PubMed ID: 5004413
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