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Journal Abstract Search

228 related items for PubMed ID: 7645599

  • 1. Autosomal dominant inheritance in Setleis syndrome.
    Masuno M, Imaizumi K, Makita Y, Nakamura M, Kuroki Y.
    Am J Med Genet; 1995 May 22; 57(1):57-60. PubMed ID: 7645599
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  • 2. Setleis (bitemporal 'forceps marks') syndrome in a German family: evidence for autosomal dominant inheritance.
    Artlich A, Schwinger E, Meinecke P.
    Clin Dysmorphol; 1992 Jul 22; 1(3):157-60. PubMed ID: 1342863
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  • 4. Setleis syndrome: three new cases and a review of the literature.
    McGaughran J, Aftimos S.
    Am J Med Genet; 2002 Sep 01; 111(4):376-80. PubMed ID: 12210295
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  • 5. Expanded phenotype and ethnicity in Setleis syndrome.
    Clark RD, Golabi M, Lacassie Y, Hall B, Seto S.
    Am J Med Genet; 1989 Nov 01; 34(3):354-7. PubMed ID: 2596524
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  • 9. Ophthalmic findings in Setleis syndrome: two new cases in a mother and son.
    Kent JS, Romanchuk KG, Lemire EG.
    Can J Ophthalmol; 2007 Jun 01; 42(3):471-3. PubMed ID: 17508049
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  • 12. Autosomal dominant inheritance of the DeMyer Sequence.
    Jaramillo C, Brandt SK, Jorgenson RJ.
    J Craniofac Genet Dev Biol; 1988 Jun 01; 8(3):199-204. PubMed ID: 3209682
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  • 16. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties.
    Colville D, Wang YY, Jamieson R, Collins F, Hood J, Savige J.
    Ophthalmic Genet; 2000 Dec 01; 21(4):217-25. PubMed ID: 11135492
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  • 19. New autosomal dominant syndrome resembling craniofrontonasal dysplasia.
    Teebi AS.
    Am J Med Genet; 1987 Nov 01; 28(3):581-91. PubMed ID: 3425628
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