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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

210 related items for PubMed ID: 11208408

  • 21. Apparent Greig cephalopolysyndactyly and sinus node disease.
    Fryns JP, De Waele P, Van der Hauwaert L, Van den Berghe H.
    Am J Med Genet; 1993 Jan 01; 45(1):38-40. PubMed ID: 8418656
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  • 24. Update on a family with hand-foot-genital syndrome: hypospadias and urinary tract abnormalities in two boys from the fourth generation.
    Donnenfeld AE, Schrager DS, Corson SL.
    Am J Med Genet; 1992 Nov 01; 44(4):482-4. PubMed ID: 1442892
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  • 25. Extending the spectrum of distal arthrogryposis.
    Gripp KW, Scott CI, Brockett BC, Nicholson L, Mackenzie WG.
    Am J Med Genet; 1996 Nov 11; 65(4):286-90. PubMed ID: 8923937
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  • 26. Daughter and her mildly affected father with Keipert syndrome.
    Dumic M, Kokic DD, Matic T, Potocki K.
    Am J Med Genet A; 2006 Nov 15; 140(22):2488-92. PubMed ID: 17036315
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  • 27. Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face.
    Winter RM.
    Am J Med Genet; 1993 Nov 01; 47(6):917-20. PubMed ID: 7506485
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  • 28. Symbrachydactyly involving hands and feet.
    De Smet L, Fabry G, Fryns JP.
    Genet Couns; 1998 Nov 01; 9(1):23-7. PubMed ID: 9555583
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  • 29. [The Tel Hashomer camptodactyly syndrome].
    Rogovina EG, Aver'ianov IuN, Nechkina NP, Logunova LV.
    Zh Nevrol Psikhiatr Im S S Korsakova; 1995 Nov 01; 95(4):83-6. PubMed ID: 8533519
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  • 32. Refinement of the deletion in 7q21.3 associated with split hand/foot malformation type 1 and Mondini dysplasia.
    Wieland I, Muschke P, Jakubiczka S, Volleth M, Freigang B, Wieacker PF.
    J Med Genet; 2004 May 01; 41(5):e54. PubMed ID: 15121782
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  • 33. Bilateral complete radioulnar synostosis associated with ectrodactyly and sensorineural hearing loss: a variant of SHFM1.
    Debeer P, Vandenbossche L, de Ravel TJ, Desloovere C, De Smet L, Huysmans C, Thoelen R, Vermeesch J, Van de Ven WJ, Fryns JP.
    Clin Genet; 2004 Feb 01; 65(2):153-5. PubMed ID: 14984476
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  • 35. The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanism.
    Keymolen K, De Smet L, Bracke P, Fryns JP.
    Genet Couns; 1999 Feb 01; 10(3):295-300. PubMed ID: 10546102
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  • 36. Two sisters with growth failure, microcephaly, peculiar facies and apical dystrophy: the presentation of brachymorphism-onychodysplasia-dysphalangism syndrome?
    Ounap K, Justus I, Lipping-Sitska M.
    Clin Dysmorphol; 1998 Jan 01; 7(1):45-50. PubMed ID: 9546830
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  • 38. Vohwinkel syndrome with mental retardation.
    Mercy P, Singh A, Ghorpade AK, Das MN, Upadhyay A, Keswani N.
    Indian J Dermatol Venereol Leprol; 2013 Jan 01; 79(5):725. PubMed ID: 23974601
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  • 40. Terminal 2q37 deletion and autistic behaviour.
    Lukusa T, Smeets E, Vogels A, Vermeesch JR, Fryns JP.
    Genet Couns; 2005 Jan 01; 16(2):179-80. PubMed ID: 16080299
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