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Pubmed for Handhelds

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Journal Abstract Search

357 related items for PubMed ID: 7468644

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  • 26. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
    Chen H, Tuck-Muller CM, Batista DA, Wertelecki W.
    Am J Med Genet; 1995 Mar 27; 56(2):219-33. PubMed ID: 7625449
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  • 28. [Trisomy 10q24--10qter].
    Dutrillaux B, Laurent C, Bernasconi S, Lejeune J.
    Ann Genet; 1975 Dec 27; 18(4):217-22. PubMed ID: 1083188
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  • 29. Trisomy 14 mosaicism: case report and review.
    Johnson VP, Aceto T, Likness C.
    Am J Med Genet; 1979 Dec 27; 3(4):331-9. PubMed ID: 474633
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  • 30. [Autosomal chromosome aberrations].
    Serville F, Battin J.
    Bord Med; 1971 May 27; 4(5):1373-416. PubMed ID: 5105683
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  • 35. Phenotype-karyotype correlations in dup(18q): report of a case and review.
    Razavi-Encha F, Raoul O, Lescs MC, Danan C.
    Am J Med Genet; 1985 Jul 27; 21(3):591-5. PubMed ID: 4025391
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  • 36. [Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].
    Ayral D, Raudrant D, Charleux JP, Noel B.
    Pediatrie; 1984 Dec 27; 39(8):681-90. PubMed ID: 6598632
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  • 39. Trisomy 20p due to a paternal reciprocal translocation.
    Funderburk SJ, Sparkes RS, Sparkes MC.
    Ann Genet; 1983 Dec 27; 26(2):94-7. PubMed ID: 6604493
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  • 40. Trisomy 18/trisomy 13 mosaicism in an adult with profound mental retardation and multiple malformations.
    Wilson WG, Shires MA, Willson KA, Wyandt HE, Harris LM, Kelly TE.
    Am J Med Genet; 1983 Sep 27; 16(1):131-6. PubMed ID: 6638063
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