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Journal Abstract Search

329 related items for PubMed ID: 8267003

  • 1. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage (Teebi-Shaltout syndrome): clinical and autopsy findings.
    Froster UG, Rehder H, Höhn W, Oberheuser F.
    Am J Med Genet; 1993 Oct 01; 47(5):717-22. PubMed ID: 8267003
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  • 2. Craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage.
    Teebi AS, Shaltout AA.
    Am J Med Genet; 1989 May 01; 33(1):58-60. PubMed ID: 2750786
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  • 9. Fryns syndrome: an autosomal recessive disorder associated with craniofacial anomalies, diaphragmatic hernia, and distal digital hypoplasia.
    Cunniff C, Jones KL, Saal HM, Stern HJ.
    Pediatrics; 1990 Apr 01; 85(4):499-504. PubMed ID: 2314962
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  • 11. Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family.
    Tylki-Szymanska A.
    Am J Med Genet; 1986 Mar 01; 23(3):759-63. PubMed ID: 3953674
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  • 12. Congenital scalp skull defects with distal limb anomalies (Adams-Oliver syndrome--McKusick 10030): further suggestion of autosomal recessive inheritance.
    Koiffmann CP, Wajntal A, Huyke BJ, Castro RM.
    Am J Med Genet; 1988 Feb 01; 29(2):263-8. PubMed ID: 3354597
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  • 13. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug 01; 33(4):479-82. PubMed ID: 2596508
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  • 16. Apparent Malpuech syndrome: report on three Brazilian patients with additional signs.
    Guion-Almeida ML.
    Am J Med Genet; 1995 Jul 31; 58(1):13-7. PubMed ID: 7573149
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  • 17. [Genetic morphological fatal syndrome. Smith-Lemli-Opitz syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 31; 14(2):91-2. PubMed ID: 8469651
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  • 19. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D, Hadley DW, Tifft CJ, Biesecker LG.
    Am J Med Genet; 2002 Jul 15; 110(4):308-14. PubMed ID: 12116202
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  • 20. Autosomal dominant inheritance of the DeMyer Sequence.
    Jaramillo C, Brandt SK, Jorgenson RJ.
    J Craniofac Genet Dev Biol; 1988 Jul 15; 8(3):199-204. PubMed ID: 3209682
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