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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

61 related items for PubMed ID: 3232711

  • 1. Developmental pathogenesis of chromosome disorders: a final word.
    Langenbeck U.
    Am J Med Genet; 1988 Oct; 31(2):479-80. PubMed ID: 3232711
    [No Abstract] [Full Text] [Related]

  • 2. Osseous malformations associated with chromosome abnormalities.
    Weiss L, Reynolds WA.
    Orthop Clin North Am; 1972 Nov; 3(3):713-32. PubMed ID: 4264453
    [No Abstract] [Full Text] [Related]

  • 3. An inherited pericentric chromosomal inversion (46, inv3 (p-q+)) associated with skeletal anomalies.
    Cohen MM, Davidson RG.
    J Pediatr; 1971 Sep; 79(3):456-62. PubMed ID: 5567968
    [No Abstract] [Full Text] [Related]

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  • 5. [Hereditary brachydactyly with nail aplasia].
    Santos HG, George FH, Ferreira JR.
    Acta Med Port; 1981 Sep; 3(2):147-60. PubMed ID: 7315521
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  • 9. [Genetics and disorders of the osseous system].
    Koulischer L.
    Acta Orthop Belg; 1965 Sep; 31(4):627-39. PubMed ID: 5846899
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  • 11. Inverted insertion of chromosome 7q and ectrodactyly.
    Naritomi K, Izumikawa Y, Tohma T, Hirayama K.
    Am J Med Genet; 1993 Jun 15; 46(5):492-3. PubMed ID: 8322806
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  • 12. [Holt syndrome: an autosomal dominant, heterogeneous, acral malformation].
    Hernández Téllez A, Corona Rivera E, Martínez-Basalo C, Nazará Cazorla Z, Aguirre-Negrete MG, Cantú JM.
    Bol Med Hosp Infant Mex; 1982 Feb 15; 39(2):131-3. PubMed ID: 7093017
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  • 17. [Symptoms of genetic significance in orthopedics].
    Kalmár L, Papp L, Mándi A.
    Beitr Orthop Traumatol; 1973 Sep 15; 20(9):502-4. PubMed ID: 4271168
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  • 18. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A.
    An Esp Pediatr; 1981 May 15; 14(5):344-51. PubMed ID: 7294523
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  • 19. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
    Giovannelli G, Forabosco A, Dutrillaux B.
    Ann Genet; 1974 Jun 15; 17(2):119-24. PubMed ID: 4547939
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