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Journal Abstract Search

247 related items for PubMed ID: 6344635

  • 1. Autosomal dominant inheritance of the Aarskog syndrome.
    Grier RE, Farrington FH, Kendig R, Mamunes P.
    Am J Med Genet; 1983 May; 15(1):39-46. PubMed ID: 6344635
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  • 4. [Aarskog's syndrome. Description of a case and endocrinological study].
    Saggese G, Bertelloni S, Baroncelli GI, Calisti L.
    Pediatr Med Chir; 1983 May; 5(6):613-8. PubMed ID: 6442411
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  • 8. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
    Teebi AS.
    Am J Med Genet; 1987 Nov; 28(3):581-91. PubMed ID: 3425628
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  • 9. New autosomal recessive faciodigitogenital syndrome.
    Teebi AS, Naguib KK, Al-Awadi S, Al-Saleh QA.
    J Med Genet; 1988 Jun; 25(6):400-6. PubMed ID: 3398008
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  • 10. The Aarskog syndrome.
    Oberiter V, Lovrencić MK, Schmutzer L, Kraus O.
    Acta Paediatr Scand; 1980 Jul; 69(4):567-70. PubMed ID: 7446107
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  • 14. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2.
    Robin NH, Feldman GJ, Aronson AL, Mitchell HF, Weksberg R, Leonard CO, Burton BK, Josephson KD, Laxová R, Aleck KA, Allanson JE, Guion-Almeida ML, Martin RA, Leichtman LG, Price RA, Opitz JM, Muenke M.
    Nat Genet; 1995 Dec; 11(4):459-61. PubMed ID: 7493033
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  • 15. Teebi hypertelorism syndrome: further observations.
    Tsukahara M, Uchida M, Shinohara T.
    Am J Med Genet; 1995 Oct 23; 59(1):59-61. PubMed ID: 8849013
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  • 16. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot.
    Jones MC, Waldman JD.
    Am J Med Genet; 1985 Sep 23; 22(1):135-41. PubMed ID: 4050848
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  • 17. Autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias.
    Guttmacher AE.
    Am J Med Genet; 1993 Apr 15; 46(2):219-22. PubMed ID: 8484413
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