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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

118 related items for PubMed ID: 2114799

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  • 2. Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II.
    Stern HJ, Graham JM, Lachman RS, Horton W, Bernini PM, Spiegel PK, Bodurtha J, Ives EJ, Bocian M, Rimoin DL.
    Am J Med Genet; 1990 Jun; 36(2):183-95. PubMed ID: 2368807
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  • 4. Hypoplasia of the transverse sinus in oto-palato-digital syndrome type I.
    Suzumura H, Kano K, Nishimura G.
    Am J Med Genet; 1998 Oct 12; 79(5):401-2. PubMed ID: 9779811
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  • 5. Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasia.
    Brewster TG, Lachman RS, Kushner DC, Holmes LB, Isler RJ, Rimoin DL.
    Am J Med Genet; 1985 Feb 12; 20(2):249-54. PubMed ID: 3976718
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  • 6. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A, Donnai D.
    Clin Dysmorphol; 1998 Jan 12; 7(1):21-7. PubMed ID: 9546826
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  • 7. Congenital constriction band syndrome.
    Perdue PS, Blanco JS, Geary W, Goitz HT.
    J South Orthop Assoc; 1996 Jan 12; 5(1):71-5. PubMed ID: 8673592
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  • 12. Vertebral anomalies in a new family with ODED syndrome.
    Piersall LD, Dowton SB, McAlister WH, Waggoner DJ.
    Clin Genet; 2000 Jun 12; 57(6):444-8. PubMed ID: 10905665
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  • 13. EEC syndrome: report on 20 new patients, clinical and genetic considerations.
    Rodini ES, Richieri-Costa A.
    Am J Med Genet; 1990 Sep 12; 37(1):42-53. PubMed ID: 2240042
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  • 14. Hunter-McAlpine syndrome: report of a third family.
    Adès LC, Morris LL, Simpson DA, Haan EA.
    Clin Dysmorphol; 1993 Apr 12; 2(2):123-30. PubMed ID: 8281273
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  • 15. Absent pituitary gland in two brothers with an oral-facial-digital syndrome resembling OFDS II and VI: a new type of OFDS?
    Shashi V, Clark P, Rogol AD, Wilson WG.
    Am J Med Genet; 1995 May 22; 57(1):22-6. PubMed ID: 7645593
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  • 17. Multiple congenital anomalies associated with an oto-palato-digital syndrome type II.
    Blanchet P, Lefort G, Eglin MC, Rieu D, Sarda P.
    Genet Couns; 1993 May 22; 4(4):289-94. PubMed ID: 8110417
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  • 18. Two isolated cases with symmetrically absent hands and feet.
    Horn D, Kolb GP.
    Clin Dysmorphol; 1994 Jul 22; 3(3):228-33. PubMed ID: 7981858
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  • 20. Acrodysplasia, severe ossification abnormalities with short stature, and fibular hypoplasia.
    Castriota-Scanderbeg A, Zelante L, Masala S, Gasparini P, Lachman RS.
    Am J Med Genet; 1999 May 07; 84(1):68-73. PubMed ID: 10213049
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