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PUBMED FOR HANDHELDS

Journal Abstract Search


189 related items for PubMed ID: 5519607

  • 1.
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  • 2. The 4p-syndrome, with a report of two new cases.
    Fryns JP, Eggermont E, Verresen H, Van den Berghe H.
    Humangenetik; 1973; 19(1):99-109. PubMed ID: 4725911
    [No Abstract] [Full Text] [Related]

  • 3. Trisomy for the short arms of chromosome 9 in two generations, with balanced translocations t(15pplus;9qminus) in three generations.
    Podruch PE, Weisskopf B.
    J Pediatr; 1974 Jul; 85(1):92-5. PubMed ID: 4855265
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  • 5. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
    Sartori A, Tenconi R, Baccichetti C, Pujatti G.
    Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
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  • 7. A child with a ring-4 chromosome (46,XX-46,XX,r 4).
    Parker CE, Alfi OS, Derencsenyi A, Mavalwala J, Donnell G.
    Am J Dis Child; 1974 Sep; 128(3):371-4. PubMed ID: 4411581
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  • 9. Ring-G chromosome, a new G-deletion syndrome?
    Weleber RG, Hecht F, Giblett ER.
    Am J Dis Child; 1968 Apr; 115(4):489-93. PubMed ID: 4296014
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  • 11. An extra small metacentric chromosome in a mentally retarded boy.
    Ishmael J, Laurence KM.
    J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
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  • 13. Chromosome aberrations in 50 patients with idiopathic mental retardation and in 50 control subjects. Madison blind study 3.
    Daly RF.
    J Pediatr; 1970 Sep; 77(3):444-53. PubMed ID: 5502094
    [No Abstract] [Full Text] [Related]

  • 14. [Giemsa-R-banding analysis of the trisomy 9p and report of a new case].
    Rethoré MO, Hoehn H, Rott HD, Couturier J, Dutrillaux B, Lejeune J.
    Humangenetik; 1973 Apr 16; 18(2):129-38. PubMed ID: 4124236
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  • 19. Partial F trisomy associated with familial F-13 translocation detected and identified by parental chromosome studies.
    Carrel RE, Sparkes RS, Wright SW.
    J Pediatr; 1971 Apr 16; 78(4):664-72. PubMed ID: 5547823
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