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Pubmed for Handhelds

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Journal Abstract Search

224 related items for PubMed ID: 8418653

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  • 2. Novel karyotype in the Ullrich-Turner syndrome--45,X/46,X,r(X)/46,X, dic(X)--investigated with fluorescence in situ hybridization.
    Robson L, Jackson J, Cowell C, Sillence D, Smith A.
    Am J Med Genet; 1994 Apr 15; 50(3):251-4. PubMed ID: 8042669
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  • 7. [Diagnosis of sex chromosome abnormality by fluorescence in-situ hybridization].
    Huang Y, Sun X, Li Q.
    Zhonghua Yi Xue Za Zhi; 1999 Feb 15; 79(2):106-8. PubMed ID: 11601014
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  • 10. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells].
    Huang Y, Sun X, Li Q.
    Zhonghua Fu Chan Ke Za Zhi; 1999 Mar 15; 34(3):153-5. PubMed ID: 11263185
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  • 16. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM, Van Tintelen JP, Stigter R, Brouwers HA, Scheres JM.
    Genet Couns; 2000 Mar 15; 11(3):241-7. PubMed ID: 11043432
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  • 18. Fluorescence in situ hybridization analysis of allelic losses involving the long arm of chromosome 17 in NF1-associated neurofibromas.
    De Luca A, Bernardini L, Ceccarini C, Sinibaldi L, Novelli A, Giustini S, Daniele I, Calvieri S, Mingarelli R.
    Cancer Genet Cytogenet; 2004 Apr 15; 150(2):168-72. PubMed ID: 15066327
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