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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

195 related items for PubMed ID: 5054315

  • 1. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
    Gustavson KH, Hitrec V, Santesson B.
    Clin Genet; 1972; 3(2):135-46. PubMed ID: 5054315
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  • 6. Trisomy 22. Two new cases and delineation of the phenotype.
    Penchaszadeh VB, Coco R.
    J Med Genet; 1975 Jun; 12(2):193-9. PubMed ID: 49427
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  • 8. An extra small metacentric chromosome in association with multiple congenital abnormalities.
    Finley WH, Finley SC, Monsky D.
    J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
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  • 11. [Abnormalities in the field of otorhinolaryngology. Genetic report].
    Jörgensen G.
    Arch Klin Exp Ohren Nasen Kehlkopfheilkd; 1972 Sep; 202(1):1-50. PubMed ID: 4260698
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  • 13. 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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  • 16. Trisomy 9 mosaicism with multiple congenital anomalies.
    Haslam RH, Broske SP, Moore CM, Thomas GH, Neill CA.
    J Med Genet; 1973 Jun; 10(2):180-4. PubMed ID: 4714587
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  • 18. Human chromosomal deletion: two patients with the 4p- syndrome.
    Arias D, Passarge E, Engle MA, German J.
    J Pediatr; 1970 Jan; 76(1):82-8. PubMed ID: 5410164
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  • 20. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Jan; 23(6):568-85. PubMed ID: 4134631
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