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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

303 related items for PubMed ID: 7204325

  • 1. A particular form of cranio-facio-mandibular dysostosis with type B brachydactylia.
    Van Damme W, Touitou D.
    J Belge Radiol; 1980; 63(4):491-6. PubMed ID: 7204325
    [No Abstract] [Full Text] [Related]

  • 2. Fronto-nasal dysostosis, callosal agenesis, crossed-fused ectopia, tibial hemimelia, and preaxial polydactyly of feet: severe expression of the acrocallosal syndrome?
    Sueldo G, Fernandes MC.
    Am J Med Genet; 1993 Jun 01; 46(4):355-7. PubMed ID: 8357003
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  • 5. [Two malformative syndromes possibly unifiable: Ullrich-Feichtiger and Smith-Lemli-Opitz syndromes. Case report].
    Lendvai D, Castello MA, Ballati G.
    Minerva Pediatr; 1969 Jan 14; 21(2):56-61. PubMed ID: 4388355
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  • 6. François' syndrome. An intermediate between mandibulofacial and craniofacial dysostoses.
    van Balen AT.
    Ophthalmic Paediatr Genet; 1985 Aug 14; 6(1-2):299-302. PubMed ID: 4069588
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  • 7. Cone-shaped epiphyses in the distal phalanges. Case report of a child with anorchia.
    Saldino RM, Marshall S, Taybi H.
    Radiol Clin Biol; 1972 Aug 14; 41(6):449-52. PubMed ID: 4404981
    [No Abstract] [Full Text] [Related]

  • 8. A case of Freeman-Sheldon syndrome (cranio-carpotarsal dysplasia) with spatulate ("canoe paddle") ribs.
    Patel M, Mahmud F.
    Br J Radiol; 1983 Jan 14; 56(661):50-1. PubMed ID: 6821743
    [No Abstract] [Full Text] [Related]

  • 9. Neonatal hyperthyroidism with accelerated skeletal maturation, craniosynostosis, and brachydactyly.
    Riggs W, Wilroy RS, Etteldorf JN.
    Radiology; 1972 Dec 14; 105(3):621-5. PubMed ID: 4642468
    [No Abstract] [Full Text] [Related]

  • 10. [The familial Miller syndrome].
    Cacchione O, Guadagni A, Persichetti B, Logoluso G, Barbuti D.
    Radiol Med; 1992 Nov 14; 84(5):650-2. PubMed ID: 1475432
    [No Abstract] [Full Text] [Related]

  • 11. [Pycnodysostosis in the radiographic picture (Toulouse Lautrec's disease--3 new cases)].
    Janecka J, Bruna J.
    Fortschr Geb Rontgenstr Nuklearmed; 1973 Mar 14; 118(3):298-305. PubMed ID: 4691615
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  • 12. [The syndrome of the first branchial arch (author's transl)].
    Boroń Z, Danilewicz-Wytrychowska T, Kolodziej M, Kolodziej M, Poprzedziński E.
    Pol Przegl Radiol Med Nukl; 1976 Mar 14; 40(4):279-83. PubMed ID: 980939
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  • 15. Robinow (fetal face) syndrome: report of a boy with dominant type and an infant with recessive type.
    Kantaputra PN, Gorlin RJ, Ukarapol N, Unachak K, Sudasna J.
    Am J Med Genet; 1999 May 07; 84(1):1-7. PubMed ID: 10213037
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  • 16. [A case of congenital hypodactyly of the hand and foot].
    Mamedov AG, Seidov MM.
    Ortop Travmatol Protez; 1991 Apr 07; (4):51-2. PubMed ID: 1754179
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  • 17. Robin sequence and oligodactyly in mother and son--probably a further example of the postaxial acrofacial dysostosis syndrome.
    Meinecke P, Wiedemann HR.
    Am J Med Genet; 1987 Aug 07; 27(4):953-7. PubMed ID: 3425604
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  • 20. [Lethal mandibulofacial and ulnofibular dysostosis].
    Poissonnier M, Neuville V, Petit P, Busuttil R.
    Ann Pediatr (Paris); 1983 Nov 07; 30(9):713-7. PubMed ID: 6686424
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